A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9757



Internal ID15540075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:114605790..114640014hg38UCSC Ensembl
Outerchr8:115618019..115652243hg19UCSC Ensembl
Outerchr8:115687195..115721419hg18UCSC Ensembl
Outerchr8:115687195..115721419hg17UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3834225
hg1934225
hg1834225
hg1734225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356
Supporting Variants
SamplesNA18507
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)nssv9757
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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