A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6059



Internal ID15191119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:27390719..27436295hg38UCSC Ensembl
Outerchr6:27358498..27404074hg19UCSC Ensembl
Outerchr6:27466477..27512053hg18UCSC Ensembl
Outerchr6:27466477..27512053hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3845577
hg1945577
hg1845577
hg1745577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5235
Supporting Variants
SamplesNA12156
Known GenesZNF391
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)nssv6059
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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