A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4935



Internal ID15542895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:98463090..98496835hg38UCSC Ensembl
Outerchr6:98910966..98944711hg19UCSC Ensembl
Outerchr6:99017687..99051432hg18UCSC Ensembl
Outerchr6:99017687..99051432hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg385516
hg195516
hg185516
hg175516
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5406
Supporting Variants
SamplesNA19129
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)nssv4935
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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