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dbVar

Database of genomic structural variation

nsv6131285

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:52

Description:nsv5563521 from Byrska-Bishop et. al 2021. 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: 286 SVs from 38 studies. See in: genome view

Remapped(Score: Perfect):184,730,523-184,730,574

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131285	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	184,730,523	184,730,574
nsv6131285	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	185,651,677	185,651,728

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17968250	line1 insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17968250	Remapped	Perfect	NC_000004.12:g.184 730523_184730574in s?	GRCh38.p12	First Pass	NC_000004.12	Chr4	184,730,523	184,730,574
nssv17968250	Submitted genomic		NC_000004.11:g.185 651677_185651728in s?	GRCh37 (hg19)		NC_000004.11	Chr4	185,651,677	185,651,728

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)
nssv17968250	0.03	192	6404

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