A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5338



Internal ID15550137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:68960809..68991468hg38UCSC Ensembl
Outerchr6:69670701..69701360hg19UCSC Ensembl
Outerchr6:69727422..69758081hg18UCSC Ensembl
Outerchr6:69727422..69758081hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3830660
hg1930660
hg1830660
hg1730660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2598
SamplesNA18555
Known GenesBAI3
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)nsv5338
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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