A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566573



Internal ID18864854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31542922..31564654hg38UCSC Ensembl
Innerchr19:32033828..32055560hg19UCSC Ensembl
Innerchr19:36725668..36747400hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3821733
hg1921733
hg1821733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057172
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566573
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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