A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9456



Internal ID15540407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:7741876..7765172hg38UCSC Ensembl
Outerchr8:7599398..7622694hg19UCSC Ensembl
Outerchr8:7636808..7660104hg18UCSC Ensembl
Outerchr8:7636808..7660104hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3823297
hg1923297
hg1823297
hg1723297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068
Supporting Variants
SamplesNA18517
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)nssv9456
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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