A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10146



Internal ID15195966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:10709398..10738629hg38UCSC Ensembl
Outerchr18:10709396..10738627hg19UCSC Ensembl
Outerchr18:10699396..10728627hg18UCSC Ensembl
Outerchr18:10699396..10728627hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3810262
hg1910262
hg1810262
hg1710262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2203
Supporting Variants
SamplesNA18956
Known GenesPIEZO2
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)nssv10146
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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