A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6472n54



Internal ID22774367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42838106..42943182hg38UCSC Ensembl
chr19:43342258..43447334hg19UCSC Ensembl
chr19:48034098..48139174hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38105077
hg19105077
hg18105077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579697, nsv579695
Samples
Known GenesPSG1, PSG10P, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6472n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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