A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523712



Internal ID15451005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:210616576..210616870hg38UCSC Ensembl
Innerchr1:210789920..210790214hg19UCSC Ensembl
Innerchr1:208856543..208856837hg18UCSC Ensembl
Innerchr1:207178315..207178609hg17UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38295
hg19295
hg18295
hg17295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699525
Samples
Known GenesHHAT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523712
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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