A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7731



Internal ID15552770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:32191712..32223409hg38UCSC Ensembl
Outerchr11:32213258..32244955hg19UCSC Ensembl
Outerchr11:32169834..32201531hg18UCSC Ensembl
Outerchr11:32169834..32201531hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg387812
hg197812
hg187812
hg177812
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10813
SamplesNA18956
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7731
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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