A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3902



Internal ID15538629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:121162384..121207035hg38UCSC Ensembl
Outerchr10:122921898..122966549hg19UCSC Ensembl
Outerchr10:122911888..122956539hg18UCSC Ensembl
Outerchr10:122911888..122956539hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3844652
hg1944652
hg1844652
hg1744652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7575
Supporting Variants
SamplesNA12878
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)nssv3902
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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