A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525118



Internal ID15105725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58972890..58996708hg38UCSC Ensembl
Innerchr20:57547945..57571763hg19UCSC Ensembl
Innerchr20:56981340..57005158hg18UCSC Ensembl
Innerchr20:56981340..57005158hg17UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3823819
hg1923819
hg1823819
hg1723819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701183
Samples
Known GenesCTSZ, NELFCD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525118
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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