A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7722



Internal ID15552760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:28965778..29026094hg38UCSC Ensembl
Outerchr11:28987325..29047641hg19UCSC Ensembl
Outerchr11:28943901..29004217hg18UCSC Ensembl
Outerchr11:28943901..29004217hg17UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3860317
hg1960317
hg1860317
hg1760317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8894, nssv1931, nssv3939, nssv9942
SamplesNA18507, NA12156, NA12878, NA18555
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)nsv7722
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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