A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698979



Internal ID15435631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41042916..41102533hg38UCSC Ensembl
Innerchr14:41512121..41571738hg19UCSC Ensembl
Innerchr14:40581871..40641488hg18UCSC Ensembl
Innerchr14:40581871..40641488hg17UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3859618
hg1959618
hg1859618
hg1759618
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523250
Supporting Variants
Samples
Known GenesLOC644919
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698979
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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