A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668424



Internal ID15058390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53419262..53502054hg38UCSC Ensembl
Innerchr19:53922515..54005308hg19UCSC Ensembl
Innerchr19:58614327..58697120hg18UCSC Ensembl
Innerchr19:58614327..58697120hg17UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3882793
hg1982794
hg1882794
hg1782794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515728
Supporting Variants
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668424
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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