A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6439



Internal ID15190739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3281213..3344732hg38UCSC Ensembl
Outerchr11:3302443..3365962hg19UCSC Ensembl
Outerchr11:3259019..3322538hg18UCSC Ensembl
Outerchr11:3259019..3322538hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3863520
hg1963520
hg1863520
hg1763520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7649
Supporting Variants
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)nssv6439
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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