A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8273



Internal ID15188905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:87071297..87093945hg38UCSC Ensembl
Outerchr6:87781015..87803663hg19UCSC Ensembl
Outerchr6:87837734..87860382hg18UCSC Ensembl
Outerchr6:87837734..87860382hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3822649
hg1922649
hg1822649
hg1722649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5385
Supporting Variants
SamplesNA12156
Known GenesCGA
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)nssv8273
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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