A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4891



Internal ID15542972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:13492807..13504313hg38UCSC Ensembl
Outerchr6:13493039..13504545hg19UCSC Ensembl
Outerchr6:13601018..13612524hg18UCSC Ensembl
Outerchr6:13601018..13612524hg17UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg387240
hg197240
hg187240
hg177240
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5205
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)nssv4891
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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