A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10763



Internal ID15542035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69509323..69543422hg38UCSC Ensembl
Outerchr10:71269079..71303178hg19UCSC Ensembl
Outerchr10:70939085..70973184hg18UCSC Ensembl
Outerchr10:70939085..70973184hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3834100
hg1934100
hg1834100
hg1734100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7021
Supporting Variants
SamplesNA18956
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)nssv10763
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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