A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8871



Internal ID15534993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133133994..133170839hg38UCSC Ensembl
Outerchr10:134947498..134984343hg19UCSC Ensembl
Outerchr10:134797488..134834333hg18UCSC Ensembl
Outerchr10:134836379..134873224hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3836846
hg1936846
hg1836846
hg1736846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7630
Supporting Variants
SamplesNA12156
Known GenesKNDC1
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)nssv8871
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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