A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9431



Internal ID15540382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:85998195..86009767hg38UCSC Ensembl
Outerchr6:86707913..86719485hg19UCSC Ensembl
Outerchr6:86764632..86776204hg18UCSC Ensembl
Outerchr6:86764632..86776204hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3811573
hg1911573
hg1811573
hg1711573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5384
Supporting Variants
SamplesNA18517
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)nssv9431
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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