A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702011



Internal ID15438663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81753206..81801601hg38UCSC Ensembl
Innerchr14:82219550..82267945hg19UCSC Ensembl
Innerchr14:81289303..81337698hg18UCSC Ensembl
Innerchr14:81289303..81337698hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3848396
hg1948396
hg1848396
hg1748396
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525823
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702011
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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