A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564683



Internal ID18862964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8862308..9007827hg38UCSC Ensembl
Innerchr19:8972984..9118503hg19UCSC Ensembl
Innerchr19:8833984..8979503hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38145520
hg19145520
hg18145520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063481
Supporting Variants
Samples
Known GenesMUC16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564683
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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