A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8254



Internal ID15535610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:63023804..63068611hg38UCSC Ensembl
Outerchr6:63733709..63778516hg19UCSC Ensembl
Outerchr6:63791668..63836475hg18UCSC Ensembl
Outerchr6:63791668..63836475hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3844808
hg1944808
hg1844808
hg1744808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5325
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)nssv8254
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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