A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10639



Internal ID15542159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:125567376..125601254hg38UCSC Ensembl
Outerchr8:126579620..126613498hg19UCSC Ensembl
Outerchr8:126648802..126682680hg18UCSC Ensembl
Outerchr8:126648802..126682680hg17UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3833879
hg1933879
hg1833879
hg1733879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377
Supporting Variants
SamplesNA18956
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)nssv10639
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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