A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4311



Internal ID15539038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:26117731..26152327hg38UCSC Ensembl
Outerchr18:23697695..23732291hg19UCSC Ensembl
Outerchr18:21951693..21986289hg18UCSC Ensembl
Outerchr18:21951693..21986289hg17UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg385152
hg195152
hg185152
hg175152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2233
Supporting Variants
SamplesNA12878
Known GenesPSMA8
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)nssv4311
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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