A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666432



Internal ID9932537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164808251..164835662hg38UCSC Ensembl
Outerchr3:164808094..164835815hg38UCSC Ensembl
Innerchr3:164526039..164553450hg19UCSC Ensembl
Outerchr3:164525882..164553603hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3827722
hg1927722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv894e199
Supporting Variantsessv6147999, essv5976855
SamplesNA19904, HG00543
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666432
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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