A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548469



Internal ID16335878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:188533017..188657215hg38UCSC Ensembl
Innerchr1:188502148..188626346hg19UCSC Ensembl
Innerchr1:186768771..186892969hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38124199
hg19124199
hg18124199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv730685
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548469
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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