A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702593



Internal ID15092559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127727525..127745104hg38UCSC Ensembl
Innerchr8:128739771..128757350hg19UCSC Ensembl
Innerchr8:128808953..128826532hg18UCSC Ensembl
Innerchr8:128808953..128826532hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3817580
hg1917580
hg1817580
hg1717580
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516713
Supporting Variants
Samples
Known GenesMYC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702593
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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