A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150592



Internal ID15509122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10814336..11662152hg38UCSC Ensembl
Innerchr18:10814334..11662151hg19UCSC Ensembl
Innerchr18:10804334..11652151hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38847817
hg19847818
hg18847818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576480
Supporting Variants
Samples1782681555_A
Known GenesMIR7153, PIEZO2, SLC35G4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150592
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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