A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6212



Internal ID15537651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:32813151..32835437hg38UCSC Ensembl
Outerchr8:32670669..32692955hg19UCSC Ensembl
Outerchr8:32790211..32812497hg18UCSC Ensembl
Outerchr8:32790211..32812497hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3822287
hg1922287
hg1822287
hg1722287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144
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)nssv6212
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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