A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10986



Internal ID15539574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:47024467..47025650hg38UCSC Ensembl
Outerchr18:44550838..44552021hg19UCSC Ensembl
Outerchr18:42804836..42806019hg18UCSC Ensembl
Outerchr18:42804836..42806019hg17UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3814506
hg1914506
hg1814506
hg1714506
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2284
Supporting Variants
SamplesNA15510
Known GenesKATNAL2
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)nssv10986
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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