A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3562536



Internal ID18860817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36460442..36556187hg38UCSC Ensembl
Innerchr17:34816256..34912028hg19UCSC Ensembl
Innerchr17:31890369..31986141hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3895746
hg1995773
hg1895773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065997
Supporting Variants
Samples
Known GenesGGNBP2, MYO19, PIGW, ZNHIT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3562536
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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