A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516476



Internal ID15443769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:83367460..83389558hg38UCSC Ensembl
Innerchr4:84288613..84310711hg19UCSC Ensembl
Innerchr4:84507637..84529735hg18UCSC Ensembl
Innerchr4:84645792..84667890hg17UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3822099
hg1922099
hg1822099
hg1722099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668598, nssv662971, nssv705402
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516476
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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