A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9331



Internal ID15193596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79011913..79021062hg38UCSC Ensembl
Outerchr18:76771913..76781062hg19UCSC Ensembl
Outerchr18:74872901..74882050hg18UCSC Ensembl
Outerchr18:74872901..74882050hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3819332
hg1919332
hg1819332
hg1719332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2377
Supporting Variants
SamplesNA18517
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)nssv9331
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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