A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524856



Internal ID15452149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136974617..137471923hg38UCSC Ensembl
Innerchr3:136693459..137190765hg19UCSC Ensembl
Innerchr3:138176149..138673455hg18UCSC Ensembl
Innerchr3:138176157..138673463hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38497307
hg19497307
hg18497307
hg17497307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700859
Samples
Known GenesIL20RB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524856
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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