A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524395



Internal ID15451688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:125026661..125026997hg38UCSC Ensembl
Innerchr12:125511207..125511543hg19UCSC Ensembl
Innerchr12:124077160..124077496hg18UCSC Ensembl
Innerchr12:124036087..124036423hg17UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38337
hg19337
hg18337
hg17337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700313
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524395
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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