A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706071



Internal ID15096037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24172317..24185384hg38UCSC Ensembl
Innerchr14:24641526..24654590hg19UCSC Ensembl
Innerchr14:23711366..23724430hg18UCSC Ensembl
Innerchr14:23711366..23724430hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3813068
hg1913065
hg1813065
hg1713065
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522667
Supporting Variants
Samples
Known GenesIPO4, REC8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706071
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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