A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5341



Internal ID15550141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:71215370..71247233hg38UCSC Ensembl
Outerchr6:71925073..71956936hg19UCSC Ensembl
Outerchr6:71981794..72013657hg18UCSC Ensembl
Outerchr6:71981794..72013657hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3831864
hg1931864
hg1831864
hg1731864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8260
SamplesNA12156
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)nsv5341
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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