A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516614



Internal ID15443907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:68602877..68610740hg38UCSC Ensembl
Innerchr14:69069594..69077457hg19UCSC Ensembl
Innerchr14:68139347..68147210hg18UCSC Ensembl
Innerchr14:68139347..68147210hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg387864
hg197864
hg187864
hg177864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699319, nssv699562, nssv656205, nssv704188, nssv697454, nssv675364, nssv656541, nssv671929, nssv669577, nssv674336, nssv674631
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516614
Frequency
Sample Size2026
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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