A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520629



Internal ID15101236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:77119161..77230169hg38UCSC Ensembl
Innerchr1:77584846..77695854hg19UCSC Ensembl
Innerchr1:77357434..77468442hg18UCSC Ensembl
Innerchr1:77296867..77407875hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38111009
hg19111009
hg18111009
hg17111009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697526
Samples
Known GenesPIGK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520629
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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