A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660137



Internal ID15050103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129756502..129805111hg38UCSC Ensembl
Innerchr7:129396342..129444951hg19UCSC Ensembl
Innerchr7:129183578..129232187hg18UCSC Ensembl
Innerchr7:128990293..129038902hg17UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3848610
hg1948610
hg1848610
hg1748610
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516024
Supporting Variants
Samples
Known GenesMIR182, MIR183, MIR96, NRF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660137
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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