A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699080



Internal ID15435732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34605816..34662656hg38UCSC Ensembl
Innerchr14:35075022..35131862hg19UCSC Ensembl
Innerchr14:34144773..34201613hg18UCSC Ensembl
Innerchr14:34144773..34201613hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3856841
hg1956841
hg1856841
hg1756841
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523334
Supporting Variants
Samples
Known GenesSNX6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699080
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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