A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1951



Internal ID15194548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93131058..93154490hg38UCSC Ensembl
Outerchr11:92864224..92887656hg19UCSC Ensembl
Outerchr11:92503872..92527304hg18UCSC Ensembl
Outerchr11:92503872..92527304hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3823433
hg1923433
hg1823433
hg1723433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv435
Supporting Variants
SamplesNA18555
Known GenesSLC36A4
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)nssv1951
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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