A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528910



Internal ID15456203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:200793914..200857641hg38UCSC Ensembl
Innerchr1:200763042..200826769hg19UCSC Ensembl
Innerchr1:199029665..199093392hg18UCSC Ensembl
Innerchr1:197494699..197558426hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3863728
hg1963728
hg1863728
hg1763728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705595
Samples
Known GenesCAMSAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528910
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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