A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527585



Internal ID15454878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120934810..121206720hg38UCSC Ensembl
Innerchr5:120270505..120542415hg19UCSC Ensembl
Innerchr5:120298404..120570314hg18UCSC Ensembl
Innerchr5:120298404..120570314hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38271911
hg19271911
hg18271911
hg17271911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704046
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527585
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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