A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8286



Internal ID15188892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:117633483..117678588hg38UCSC Ensembl
Outerchr6:117954646..117999751hg19UCSC Ensembl
Outerchr6:118061339..118106444hg18UCSC Ensembl
Outerchr6:118061339..118106444hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3845106
hg1945106
hg1845106
hg1745106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449
Supporting Variants
SamplesNA12156
Known GenesNUS1
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)nssv8286
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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