A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525693



Internal ID15106300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10634068..10780848hg38UCSC Ensembl
Innerchr1:10694125..10840905hg19UCSC Ensembl
Innerchr1:10616712..10763492hg18UCSC Ensembl
Innerchr1:10628391..10775171hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38146781
hg19146781
hg18146781
hg17146781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701852
Samples
Known GenesCASZ1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525693
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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