A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6474



Internal ID15190704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93122961..93154727hg38UCSC Ensembl
Outerchr11:92856127..92887893hg19UCSC Ensembl
Outerchr11:92495775..92527541hg18UCSC Ensembl
Outerchr11:92495775..92527541hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3831767
hg1931767
hg1831767
hg1731767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv435
Supporting Variants
SamplesNA12156
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)nssv6474
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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