A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6278



Internal ID15537585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6365844..6386492hg38UCSC Ensembl
Outerchr10:6407806..6428454hg19UCSC Ensembl
Outerchr10:6447812..6468460hg18UCSC Ensembl
Outerchr10:6447812..6468460hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3820649
hg1920649
hg1820649
hg1720649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5676
Supporting Variants
SamplesNA12156
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)nssv6278
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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