A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621523



Internal ID7008391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112894321..112902311hg38UCSC Ensembl
Innerchr9:112894321..112902311hg38UCSC Ensembl
Outerchr9:112894308..112902320hg38UCSC Ensembl
chr9:115656601..115664591hg19UCSC Ensembl
Innerchr9:115656601..115664591hg19UCSC Ensembl
Outerchr9:115656588..115664600hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg387991
hg197991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606327
SamplesNA19428
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621523
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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