A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515790



Internal ID15442847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167886539..168066892hg38UCSC Ensembl
Innerchr4:168807690..168988043hg19UCSC Ensembl
Innerchr4:169044265..169224618hg18UCSC Ensembl
Innerchr4:169182420..169362773hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38180354
hg19180354
hg18180354
hg17180354
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656520, nssv664790, nssv665973, nssv655070, nssv685103, nssv663585, nssv684032, nssv677677, nssv689518, nssv661639, nssv687620, nssv691921, nssv680540, nssv672599, nssv660387, nssv679806, nssv660520, nssv675352, nssv677876, nssv668388, nssv698937, nssv697528, nssv689682, nssv682889, nssv693234, nssv682608, nssv681065, nssv679342, nssv672424, nssv683058
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515790
Frequency
Sample Size2026
Observed Gain21
Observed Loss9
Observed Complex0
Frequencyn/a


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