A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525026



Internal ID15452319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31443644..31455383hg38UCSC Ensembl
Innerchr21:32815957..32827696hg19UCSC Ensembl
Innerchr21:31737828..31749567hg18UCSC Ensembl
Innerchr21:31737828..31749567hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3811740
hg1911740
hg1811740
hg1711740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701066
Samples
Known GenesTIAM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525026
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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