A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696637



Internal ID15086603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24020396..24060428hg38UCSC Ensembl
Innerchr14:24489605..24529637hg19UCSC Ensembl
Innerchr14:23559445..23599477hg18UCSC Ensembl
Innerchr14:23559445..23599477hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3840033
hg1940033
hg1840033
hg1740033
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516023
Supporting Variants
Samples
Known GenesDHRS4L1, LRRC16B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696637
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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