A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658922



Internal ID15048888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143917935..143985257hg38UCSC Ensembl
Innerchr8:144992103..145059425hg19UCSC Ensembl
Innerchr8:145064091..145131413hg18UCSC Ensembl
Innerchr8:145064091..145131413hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3867323
hg1967323
hg1867323
hg1767323
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515809
Supporting Variants
Samples
Known GenesMIR661, PARP10, PLEC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658922
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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