A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv758784



Internal ID15706054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114041494..114047023hg38UCSC Ensembl
Innerchr10:115801253..115806782hg19UCSC Ensembl
Innerchr10:115791243..115796772hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385530
hg195530
hg185530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552203
Supporting Variants
Samples
Known GenesADRB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv758784
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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