A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9692



Internal ID15540111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:76718587..76759435hg38UCSC Ensembl
Outerchr6:77428304..77469152hg19UCSC Ensembl
Outerchr6:77485023..77525871hg18UCSC Ensembl
Outerchr6:77485023..77525871hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3840849
hg1940849
hg1840849
hg1740849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5359
Supporting Variants
SamplesNA18507
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)nssv9692
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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