A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692079



Internal ID15082045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43071722..43304322hg38UCSC Ensembl
Innerchr19:43575874..43808474hg19UCSC Ensembl
Innerchr19:48267714..48500314hg18UCSC Ensembl
Innerchr19:48267714..48500314hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38232601
hg19232601
hg18232601
hg17232601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesLOC284344, PSG2, PSG4, PSG5, PSG9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692079
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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