A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549391



Internal ID16336800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:235219873..235260292hg38UCSC Ensembl
Innerchr1:235383188..235423607hg19UCSC Ensembl
Innerchr1:233449811..233490230hg18UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3840420
hg1940420
hg1840420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv738180
Samples
Known GenesARID4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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