A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663777



Internal ID15400429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45892681..46155176hg38UCSC Ensembl
Innerchr14:46361884..46624379hg19UCSC Ensembl
Innerchr14:45431634..45694129hg18UCSC Ensembl
Innerchr14:45431634..45694129hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38262496
hg19262496
hg18262496
hg17262496
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516946
Supporting Variants
Samples
Known GenesLINC00871
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663777
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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