A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6764



Internal ID15537099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:72964090..72981785hg38UCSC Ensembl
Outerchr18:70631325..70649020hg19UCSC Ensembl
Outerchr18:68782305..68800000hg18UCSC Ensembl
Outerchr18:68782305..68800000hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3812298
hg1912298
hg1812298
hg1712298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2352
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)nssv6764
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer