A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv461



Internal ID15549336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:101663376..101713273hg38UCSC Ensembl
Outerchr11:101534107..101584004hg19UCSC Ensembl
Outerchr11:101039317..101089214hg18UCSC Ensembl
Outerchr11:101039317..101089214hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3849898
hg1949898
hg1849898
hg1749898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6478, nssv3985, nssv1958, nssv9274, nssv1034, nssv10835, nssv5375
SamplesNA12156, NA12878, NA18956, NA18555, NA18517, NA19240, NA19129
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)nsv461
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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