A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8306



Internal ID15188872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:142123126..142143234hg38UCSC Ensembl
Outerchr6:142444263..142464371hg19UCSC Ensembl
Outerchr6:142485956..142506064hg18UCSC Ensembl
Outerchr6:142485956..142506064hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg385865
hg195865
hg185865
hg175865
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510
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)nssv8306
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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