A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692



Internal ID15538420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:136144504..136159559hg38UCSC Ensembl
Outerchr8:137156747..137171802hg19UCSC Ensembl
Outerchr8:137225929..137240984hg18UCSC Ensembl
Outerchr8:137225929..137240984hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3815056
hg1915056
hg1815056
hg1715056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6414
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)nssv3692
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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