A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7704



Internal ID15552740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:21017435..21062399hg38UCSC Ensembl
Outerchr11:21038981..21083945hg19UCSC Ensembl
Outerchr11:20995557..21040521hg18UCSC Ensembl
Outerchr11:20995557..21040521hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3844965
hg1944965
hg1844965
hg1744965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8889
SamplesNA12156
Known GenesNELL1
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)nsv7704
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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