A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8792



Internal ID15535072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69515451..69560423hg38UCSC Ensembl
Outerchr10:71275207..71320179hg19UCSC Ensembl
Outerchr10:70945213..70990185hg18UCSC Ensembl
Outerchr10:70945213..70990185hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3844973
hg1944973
hg1844973
hg1744973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7021
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)nssv8792
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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