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dbVar

Database of genomic structural variation

nsv3169121

Organism: Homo sapiens

Study:nstd158 (Cleal et al. 2019)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:33,202

Publication(s):Cleal et al. 2019

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: 210 SVs from 43 studies. See in: genome view

Remapped(Score: Perfect):67,908,729-67,941,936

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3169121	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	67,908,732 (-3, +3)	67,941,933 (-3, +3)
nsv3169121	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	67,959,156 (-3, +3)	67,992,357 (-3, +3)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14239846	inversion	DB111	Sequencing	Paired-end mapping	43

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14239846	Remapped	Perfect	NC_000003.12:g.(67 908729_67908735)_( 67941930_67941936) inv244	GRCh38.p12	First Pass	NC_000003.12	Chr3	67,908,732 (-3, +3)	67,941,933 (-3, +3)
nssv14239846	Submitted genomic		NC_000003.11:g.(67 959153_67959159)_( 67992354_67992360) inv244	GRCh37 (hg19)		NC_000003.11	Chr3	67,959,156 (-3, +3)	67,992,357 (-3, +3)

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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