A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523400



Internal ID15450693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116388669..116390094hg38UCSC Ensembl
Innerchr5:115724366..115725791hg19UCSC Ensembl
Innerchr5:115752265..115753690hg18UCSC Ensembl
Innerchr5:115752265..115753690hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381426
hg191426
hg181426
hg171426
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699151
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523400
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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