A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3881



Internal ID15538608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69486712..69498167hg38UCSC Ensembl
Outerchr10:71246468..71257923hg19UCSC Ensembl
Outerchr10:70916474..70927929hg18UCSC Ensembl
Outerchr10:70916474..70927929hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3811456
hg1911456
hg1811456
hg1711456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7021
Supporting Variants
SamplesNA12878
Known GenesTSPAN15
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)nssv3881
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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