A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7748



Internal ID15552788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:42100985..42145980hg38UCSC Ensembl
Outerchr11:42122535..42167530hg19UCSC Ensembl
Outerchr11:42079111..42124106hg18UCSC Ensembl
Outerchr11:42079111..42124106hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3844996
hg1944996
hg1844996
hg1744996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8900
SamplesNA12156
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)nsv7748
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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