A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8278



Internal ID15535586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:97628283..97661306hg38UCSC Ensembl
Outerchr6:98076159..98109182hg19UCSC Ensembl
Outerchr6:98182880..98215903hg18UCSC Ensembl
Outerchr6:98182880..98215903hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg386410
hg196410
hg186410
hg176410
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5403
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)nssv8278
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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