A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665728



Internal ID15055694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42897784..43071722hg38UCSC Ensembl
Innerchr19:43401936..43575874hg19UCSC Ensembl
Innerchr19:48093776..48267714hg18UCSC Ensembl
Innerchr19:48093776..48267714hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38173939
hg19173939
hg18173939
hg17173939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesPSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665728
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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