A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6066



Internal ID15191112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:54045080..54087432hg38UCSC Ensembl
Outerchr6:53909878..53952230hg19UCSC Ensembl
Outerchr6:54017837..54060189hg18UCSC Ensembl
Outerchr6:54017837..54060189hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3842353
hg1942353
hg1842353
hg1742353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5307
Supporting Variants
SamplesNA12156
Known GenesMLIP
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)nssv6066
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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