A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697789



Internal ID15434441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:91084547..91089203hg38UCSC Ensembl
Innerchr14:91550891..91555547hg19UCSC Ensembl
Innerchr14:90620644..90625300hg18UCSC Ensembl
Innerchr14:90620644..90625300hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg384657
hg194657
hg184657
hg174657
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521104
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697789
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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