A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7656



Internal ID15206001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:6261874..6306596hg38UCSC Ensembl
Outerchr11:6283104..6327826hg19UCSC Ensembl
Outerchr11:6239680..6284402hg18UCSC Ensembl
Outerchr11:6239680..6284402hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3844723
hg1944723
hg1844723
hg1744723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8876
SamplesNA12156
Known GenesCCKBR
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)nsv7656
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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