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dbVar

Database of genomic structural variation

nsv499704

Organism: Homo sapiens

Study:nstd47 (Kidd et al. 2010b)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,543

Publication(s):Kidd et al. 2010

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: 337 SVs from 52 studies. See in: genome view

Remapped(Score: Perfect):3,975,898-3,977,440

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499704	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	3,975,898	3,977,440
nsv499704	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	4,015,530	4,017,072
nsv499704	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000007.12	Chr7	3,982,056	3,983,598

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585627	copy number gain	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585627	Remapped	Perfect	NC_000007.14:g.397 5898_3977440dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	3,975,898	3,977,440
nssv585627	Remapped	Perfect	NC_000007.13:g.401 5530_4017072dup	GRCh37.p13	First Pass	NC_000007.13	Chr7	4,015,530	4,017,072
nssv585627	Submitted genomic		NC_000007.12:g.398 2056_3983598dup	NCBI36 (hg18)		NC_000007.12	Chr7	3,982,056	3,983,598

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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