A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690823



Internal ID15080789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127735225..127738294hg38UCSC Ensembl
Innerchr8:128747471..128750540hg19UCSC Ensembl
Innerchr8:128816653..128819722hg18UCSC Ensembl
Innerchr8:128816653..128819722hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg383070
hg193070
hg183070
hg173070
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)nssv690823
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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