A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702838



Internal ID15439490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27142523..27156494hg38UCSC Ensembl
Innerchr7:27182142..27196113hg19UCSC Ensembl
Innerchr7:27148667..27162638hg18UCSC Ensembl
Innerchr7:26955382..26969353hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3813972
hg1913972
hg1813972
hg1713972
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526526
Supporting Variants
Samples
Known GenesHOXA5, HOXA6, HOXA7, HOXA-AS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702838
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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