A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516889



Internal ID15444182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98735238..98737467hg38UCSC Ensembl
Innerchr14:99201575..99203804hg19UCSC Ensembl
Innerchr14:98271328..98273557hg18UCSC Ensembl
Innerchr14:98271328..98273557hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382230
hg192230
hg182230
hg172230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679112, nssv654723
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516889
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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