A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688652



Internal ID15425304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20893225..20945443hg38UCSC Ensembl
Innerchr14:21361384..21413602hg19UCSC Ensembl
Innerchr14:20431224..20483442hg18UCSC Ensembl
Innerchr14:20431224..20483442hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3852219
hg1952219
hg1852219
hg1752219
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)nssv688652
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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