A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569650



Internal ID18867931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42816973..43056212hg38UCSC Ensembl
Innerchr19:43321125..43560364hg19UCSC Ensembl
Innerchr19:48012965..48252204hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38239240
hg19239240
hg18239240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057231
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3569650
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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