A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520019



Internal ID15447312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:61157352..61159399hg38UCSC Ensembl
Innerchr14:61624070..61626117hg19UCSC Ensembl
Innerchr14:60693823..60695870hg18UCSC Ensembl
Innerchr14:60693823..60695870hg17UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg382048
hg192048
hg182048
hg172048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697180
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520019
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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