A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777



Internal ID15544494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:134069034..134092233hg38UCSC Ensembl
Outerchr8:135081277..135104476hg19UCSC Ensembl
Outerchr8:135150459..135173658hg18UCSC Ensembl
Outerchr8:135150459..135173658hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3823200
hg1923200
hg1823200
hg1723200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407
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)nssv777
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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