A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4928



Internal ID15542908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:82257154..82276998hg38UCSC Ensembl
Outerchr6:82966871..82986715hg19UCSC Ensembl
Outerchr6:83023590..83043434hg18UCSC Ensembl
Outerchr6:83023590..83043434hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3810594
hg1910594
hg1810594
hg1710594
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5373
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)nssv4928
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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