A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692116



Internal ID15428768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20893225..20952929hg38UCSC Ensembl
Innerchr14:21361384..21421088hg19UCSC Ensembl
Innerchr14:20431224..20490928hg18UCSC Ensembl
Innerchr14:20431224..20490928hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3859705
hg1959705
hg1859705
hg1759705
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517174
Supporting Variants
Samples
Known GenesECRP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692116
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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