A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701124



Internal ID15437776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39833672..39884552hg38UCSC Ensembl
Innerchr14:40302876..40353756hg19UCSC Ensembl
Innerchr14:39372627..39423507hg18UCSC Ensembl
Innerchr14:39372627..39423507hg17UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3850881
hg1950881
hg1850881
hg1750881
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525070
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701124
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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