A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657813



Internal ID15047779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16015985..16036926hg38UCSC Ensembl
Innerchr19:16126795..16147736hg19UCSC Ensembl
Innerchr19:15987795..16008736hg18UCSC Ensembl
Innerchr19:15987795..16008736hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3820942
hg1920942
hg1820942
hg1720942
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517514
Supporting Variants
Samples
Known GenesLINC00661, LINC00905
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657813
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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