A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710



Internal ID15538438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:32934698..32951230hg38UCSC Ensembl
Outerchr9:32934696..32951228hg19UCSC Ensembl
Outerchr9:32924696..32941228hg18UCSC Ensembl
Outerchr9:32924696..32941228hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg385987
hg195987
hg185987
hg175987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522
Supporting Variants
SamplesNA12878
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)nssv3710
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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