A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3462



Internal ID15538190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:103288737..103323020hg38UCSC Ensembl
Outerchr6:103736612..103770895hg19UCSC Ensembl
Outerchr6:103843305..103877588hg18UCSC Ensembl
Outerchr6:103843305..103877588hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3834284
hg1934284
hg1834284
hg1734284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415
Supporting Variants
SamplesNA12878
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)nssv3462
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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