A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522542



Internal ID15103149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119588083..119590413hg38UCSC Ensembl
Innerchr3:119306930..119309260hg19UCSC Ensembl
Innerchr3:120789620..120791950hg18UCSC Ensembl
Innerchr3:120789620..120791950hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382331
hg192331
hg182331
hg172331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705921
Samples
Known GenesADPRH
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522542
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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