A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695003



Internal ID15084969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10771437..10777807hg38UCSC Ensembl
Innerchr8:10628947..10635317hg19UCSC Ensembl
Innerchr8:10666357..10672727hg18UCSC Ensembl
Innerchr8:10666357..10672727hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386371
hg196371
hg186371
hg176371
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522226
Supporting Variants
Samples
Known GenesPINX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695003
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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