A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8266



Internal ID15535598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:76363214..76396490hg38UCSC Ensembl
Outerchr6:77072931..77106207hg19UCSC Ensembl
Outerchr6:77129651..77162927hg18UCSC Ensembl
Outerchr6:77129651..77162927hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3833277
hg1933277
hg1833277
hg1733277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5358
Supporting Variants
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)nssv8266
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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