A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704366



Internal ID15094332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14469516..14503430hg38UCSC Ensembl
Innerchr19:14580328..14614242hg19UCSC Ensembl
Innerchr19:14441328..14475242hg18UCSC Ensembl
Innerchr19:14441328..14475242hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3833915
hg1933915
hg1833915
hg1733915
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527867
Supporting Variants
Samples
Known GenesGIPC1, PKN1, PTGER1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704366
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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