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dbVar

Database of genomic structural variation

nsv4727237

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:insertion
Method Type:Curated
Submitted on:GRCh37

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

Description:nsv4684747 from Lee et. al 2020. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

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: 121 SVs from 24 studies. See in: genome view

Remapped(Score: Perfect):9,093,830-9,093,830

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4727237	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	9,093,830	9,093,830
nsv4727237	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000012.11	Chr12	9,246,426	9,246,426

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16252747	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16252747	Remapped	Perfect	NC_000012.12:g.909 3830_9093831ins?	GRCh38.p12	First Pass	NC_000012.12	Chr12	9,093,830	9,093,830
nssv16252747	Submitted genomic		NC_000012.11:g.924 6426_9246427ins?	GRCh37 (hg19)		NC_000012.11	Chr12	9,246,426	9,246,426

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16252747	0.819	3621	4424

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