A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524853



Internal ID15452146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:204792229..204803609hg38UCSC Ensembl
Innerchr1:204761357..204772737hg19UCSC Ensembl
Innerchr1:203027980..203039360hg18UCSC Ensembl
Innerchr1:201493014..201504394hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3811381
hg1911381
hg1811381
hg1711381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700856
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524853
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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