A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524620



Internal ID15451913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:19530786..19681217hg38UCSC Ensembl
Innerchr12:19683720..19834151hg19UCSC Ensembl
Innerchr12:19574987..19725418hg18UCSC Ensembl
Innerchr12:19574987..19725418hg17UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38150432
hg19150432
hg18150432
hg17150432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700581
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524620
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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