A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519224



Internal ID15099831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71397295..71504834hg38UCSC Ensembl
Innerchr11:71108341..71215880hg19UCSC Ensembl
Innerchr11:70785989..70893528hg18UCSC Ensembl
Innerchr11:70785989..70893528hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38107540
hg19107540
hg18107540
hg17107540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv74n21
Supporting Variantsnssv696713
Samples
Known GenesDHCR7, FLJ42102, MIR6754, NADSYN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519224
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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