A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519601



Internal ID15446894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13780343..13817610hg38UCSC Ensembl
Innerchr7:13819968..13857235hg19UCSC Ensembl
Innerchr7:13786493..13823760hg18UCSC Ensembl
Innerchr7:13593208..13630475hg17UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3837268
hg1937268
hg1837268
hg1737268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658236, nssv657010
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519601
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer