A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8495



Internal ID15535369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:56422137..56434927hg38UCSC Ensembl
Outerchr8:57334696..57347486hg19UCSC Ensembl
Outerchr8:57497250..57510040hg18UCSC Ensembl
Outerchr8:57497250..57510040hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3812791
hg1912791
hg1812791
hg1712791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6201
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)nssv8495
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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