A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10623



Internal ID15542175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:57069887..57079354hg38UCSC Ensembl
Outerchr8:57982446..57991913hg19UCSC Ensembl
Outerchr8:58145000..58154467hg18UCSC Ensembl
Outerchr8:58145000..58154467hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg386352
hg196352
hg186352
hg176352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6205
Supporting Variants
SamplesNA18956
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)nssv10623
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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