A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528986



Internal ID15109593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36689261..36692010hg38UCSC Ensembl
Innerchr5:36689363..36692112hg19UCSC Ensembl
Innerchr5:36725120..36727869hg18UCSC Ensembl
Innerchr5:36725120..36727869hg17UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg382750
hg192750
hg182750
hg172750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705686
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528986
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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