A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591247



Internal ID16378656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:106618723..106824119hg38UCSC Ensembl
Innerchr3:106337570..106542966hg19UCSC Ensembl
Innerchr3:107820260..108025656hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38205397
hg19205397
hg18205397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152519
SamplesNINDS_45
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591247
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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