A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524387



Internal ID15104994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44698642..44699855hg38UCSC Ensembl
Innerchr21:46118557..46119770hg19UCSC Ensembl
Innerchr21:44942985..44944198hg18UCSC Ensembl
Innerchr21:44942985..44944198hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381214
hg191214
hg181214
hg171214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700304
Samples
Known GenesTSPEAR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524387
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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