A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701887



Internal ID15091853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100634249..100737898hg38UCSC Ensembl
Innerchr14:101100586..101204235hg19UCSC Ensembl
Innerchr14:100170339..100273988hg18UCSC Ensembl
Innerchr14:100170339..100273988hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38103650
hg19103650
hg18103650
hg17103650
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525723
Supporting Variants
Samples
Known GenesDLK1, LINC00523
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701887
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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