A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515626



Internal ID15096233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184460429..184460907hg38UCSC Ensembl
Innerchr4:185381583..185382061hg19UCSC Ensembl
Innerchr4:185618577..185619055hg18UCSC Ensembl
Innerchr4:185756732..185757210hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38479
hg19479
hg18479
hg17479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664147, nssv660343
Samples
Known GenesIRF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515626
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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