A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv831



Internal ID15544741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:118618643..118637640hg38UCSC Ensembl
Outerchr9:121380921..121399918hg19UCSC Ensembl
Outerchr9:120420742..120439739hg18UCSC Ensembl
Outerchr9:118460475..118479472hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg386153
hg196153
hg186153
hg176153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6692
Supporting Variants
SamplesNA19240
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)nssv831
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