A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8618



Internal ID15535246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:81319320..81359579hg38UCSC Ensembl
Outerchr9:83934235..83974494hg19UCSC Ensembl
Outerchr9:83124055..83164314hg18UCSC Ensembl
Outerchr9:81163789..81204048hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3840260
hg1940260
hg1840260
hg1740260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6580
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)nssv8618
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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