A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455



Internal ID15550266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:119473811..119518471hg38UCSC Ensembl
Outerchr6:119794976..119839636hg19UCSC Ensembl
Outerchr6:119836675..119881335hg18UCSC Ensembl
Outerchr6:119836675..119881335hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3844661
hg1944661
hg1844661
hg1744661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8289
SamplesNA12156
Known GenesLOC285762
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)nsv5455
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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