A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2627



Internal ID15540485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:164120391..164138483hg38UCSC Ensembl
Outerchr6:164541423..164559515hg19UCSC Ensembl
Outerchr6:164461413..164479505hg18UCSC Ensembl
Outerchr6:164511834..164529926hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3818093
hg1918093
hg1818093
hg1718093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5583
Supporting Variants
SamplesNA18555
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)nssv2627
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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