A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545775



Internal ID15986498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23874034..23874604hg38UCSC Ensembl
Innerchr1:24200524..24201094hg19UCSC Ensembl
Innerchr1:24073111..24073681hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38571
hg19571
hg18571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv190n54
Supporting Variantsnssv711329
Samples
Known GenesCNR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545775
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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