A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7726



Internal ID15552764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:31657579..31703183hg38UCSC Ensembl
Outerchr11:31679127..31724731hg19UCSC Ensembl
Outerchr11:31635703..31681307hg18UCSC Ensembl
Outerchr11:31635703..31681307hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3845605
hg1945605
hg1845605
hg1745605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6455
SamplesNA12156
Known GenesELP4
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)nsv7726
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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