A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv581



Internal ID15545315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:133017384..133033179hg38UCSC Ensembl
Outerchr6:133338523..133354318hg19UCSC Ensembl
Outerchr6:133380216..133396011hg18UCSC Ensembl
Outerchr6:133380216..133396011hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3815796
hg1915796
hg1815796
hg1715796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481
Supporting Variants
SamplesNA19240
Known Genes
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)nssv581
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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