A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9696



Internal ID15540107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:85997801..86010782hg38UCSC Ensembl
Outerchr6:86707519..86720500hg19UCSC Ensembl
Outerchr6:86764238..86777219hg18UCSC Ensembl
Outerchr6:86764238..86777219hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3812982
hg1912982
hg1812982
hg1712982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5384
Supporting Variants
SamplesNA18507
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)nssv9696
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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