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dbVar

Database of genomic structural variation

esv2421255

Organism: Homo sapiens

Study:estd194 (Bentley et al. 2008)
Variant Type:insertion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Bentley et al. 2008

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 190 SVs from 19 studies. See in: genome view

Remapped(Score: Perfect):25,223,692-25,223,692

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv2421255	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	25,223,692	25,223,692
esv2421255	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	22,803,656	22,803,656
esv2421255	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000018.8	Chr18	21,057,654	21,057,654

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv4985492	insertion	NA18507	Sequencing	Split read mapping	504,912

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv4985492	Remapped	Perfect	NC_000018.10:g.252 23692_25223693insA	GRCh38.p12	First Pass	NC_000018.10	Chr18	25,223,692	25,223,692
essv4985492	Remapped	Perfect	NC_000018.9:g.2280 3656_22803657insA	GRCh37.p13	First Pass	NC_000018.9	Chr18	22,803,656	22,803,656
essv4985492	Submitted genomic		NC_000018.8:g.2105 7654_21057655insA	NCBI36 (hg18)		NC_000018.8	Chr18	21,057,654	21,057,654

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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