A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4896



Internal ID15542963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:19754749..19772088hg38UCSC Ensembl
Outerchr6:19754980..19772319hg19UCSC Ensembl
Outerchr6:19862959..19880298hg18UCSC Ensembl
Outerchr6:19862959..19880298hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3817340
hg1917340
hg1817340
hg1717340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5219
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)nssv4896
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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