A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv435



Internal ID15202364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93120600..93154727hg38UCSC Ensembl
Outerchr11:92853766..92887893hg19UCSC Ensembl
Outerchr11:92493414..92527541hg18UCSC Ensembl
Outerchr11:92493414..92527541hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3834128
hg1934128
hg1834128
hg1734128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6474, nssv1951, nssv3979
SamplesNA12156, NA12878, NA18555
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)nsv435
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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