A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524494



Internal ID15105101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:52593454..52715898hg38UCSC Ensembl
Innerchr4:53459620..53582065hg19UCSC Ensembl
Innerchr4:53154377..53276822hg18UCSC Ensembl
Innerchr4:53300548..53422993hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38122445
hg19122446
hg18122446
hg17122446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700432
Samples
Known GenesDANCR, MIR4449, SNORA26, USP46
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524494
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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