A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519700



Internal ID15100307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76926607..76998751hg38UCSC Ensembl
Innerchr11:76637651..76709795hg19UCSC Ensembl
Innerchr11:76315299..76387443hg18UCSC Ensembl
Innerchr11:76315299..76387443hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3872145
hg1972145
hg1872145
hg1772145
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674899, nssv688546, nssv689966, nssv661250, nssv661595, nssv704507, nssv683071, nssv657654
Samples
Known GenesACER3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519700
Frequency
Sample Size2026
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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