A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3365



Internal ID15538093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:84650588..84660888hg38UCSC Ensembl
Outerchr5:83946406..83956706hg19UCSC Ensembl
Outerchr5:83982162..83992462hg18UCSC Ensembl
Outerchr5:83982162..83992462hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3810301
hg1910301
hg1810301
hg1710301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4907
Supporting Variants
SamplesNA12878
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)nssv3365
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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