A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3456



Internal ID15538184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:85989847..86018206hg38UCSC Ensembl
Outerchr6:86699565..86727924hg19UCSC Ensembl
Outerchr6:86756284..86784643hg18UCSC Ensembl
Outerchr6:86756284..86784643hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3828360
hg1928360
hg1828360
hg1728360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5384
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)nssv3456
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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