A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10151



Internal ID15542647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:22542189..22552327hg38UCSC Ensembl
Outerchr18:20122152..20132290hg19UCSC Ensembl
Outerchr18:18376150..18386288hg18UCSC Ensembl
Outerchr18:18376150..18386288hg17UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg387518
hg197518
hg187518
hg177518
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2224
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)nssv10151
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