A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2362



Internal ID15546925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:76059850..76066768hg38UCSC Ensembl
Outerchr18:73771805..73778723hg19UCSC Ensembl
Outerchr18:71900793..71907711hg18UCSC Ensembl
Outerchr18:71900793..71907711hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg386775
hg196775
hg186775
hg176775
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10167
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)nsv2362
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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