A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515943



Internal ID15096550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87811540..87811759hg38UCSC Ensembl
Innerchr4:88732692..88732911hg19UCSC Ensembl
Innerchr4:88951716..88951935hg18UCSC Ensembl
Innerchr4:89089871..89090090hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38220
hg19220
hg18220
hg17220
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665396, nssv685671, nssv701677
Samples
Known GenesIBSP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515943
Frequency
Sample Size2026
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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