A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8475



Internal ID15535389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:25571025..25615748hg38UCSC Ensembl
Outerchr8:25428541..25473264hg19UCSC Ensembl
Outerchr8:25484458..25529181hg18UCSC Ensembl
Outerchr8:25484458..25529181hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3844724
hg1944724
hg1844724
hg1744724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6126
Supporting Variants
SamplesNA12156
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)nssv8475
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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