A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527708



Internal ID15455001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76648678..76652773hg38UCSC Ensembl
Innerchr11:76359722..76363817hg19UCSC Ensembl
Innerchr11:76037370..76041465hg18UCSC Ensembl
Innerchr11:76037370..76041465hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384096
hg194096
hg184096
hg174096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704187
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527708
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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