A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8532



Internal ID15188646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:98209446..98251459hg38UCSC Ensembl
Outerchr8:99221674..99263687hg19UCSC Ensembl
Outerchr8:99290850..99332863hg18UCSC Ensembl
Outerchr8:99290850..99332863hg17UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3842014
hg1942014
hg1842014
hg1742014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326
Supporting Variants
SamplesNA12156
Known GenesNIPAL2
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)nssv8532
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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