A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3882



Internal ID15538609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69514312..69549715hg38UCSC Ensembl
Outerchr10:71274068..71309471hg19UCSC Ensembl
Outerchr10:70944074..70979477hg18UCSC Ensembl
Outerchr10:70944074..70979477hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3835404
hg1935404
hg1835404
hg1735404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7021
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)nssv3882
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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