A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674161



Internal ID15410813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99675352..99683165hg38UCSC Ensembl
Innerchr14:100141689..100149502hg19UCSC Ensembl
Innerchr14:99211442..99219255hg18UCSC Ensembl
Innerchr14:99211442..99219255hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg387814
hg197814
hg187814
hg177814
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519710
Supporting Variants
Samples
Known GenesHHIPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674161
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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