A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528620



Internal ID15109227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70296786..70430316hg38UCSC Ensembl
Innerchr4:71162503..71296033hg19UCSC Ensembl
Innerchr4:71197092..71330622hg18UCSC Ensembl
Innerchr4:71343263..71476793hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38133531
hg19133531
hg18133531
hg17133531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv321n21
Supporting Variantsnssv705249
Samples
Known GenesCABS1, PROL1, SMR3A, SMR3B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528620
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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