A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711336



Internal ID15658606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23874282..23874772hg38UCSC Ensembl
Innerchr1:24200772..24201262hg19UCSC Ensembl
Innerchr1:24073359..24073849hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38491
hg19491
hg18491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545779
Supporting Variants
Samples
Known GenesCNR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv711336
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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