A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597929



Internal ID6985066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139028555..139066961hg38UCSC Ensembl
Innerchr3:139028555..139066961hg38UCSC Ensembl
Outerchr3:139028055..139067461hg38UCSC Ensembl
chr3:138747397..138785803hg19UCSC Ensembl
Innerchr3:138747397..138785803hg19UCSC Ensembl
Outerchr3:138746897..138786303hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3838407
hg1938407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11160808
SamplesHG01851
Known GenesPRR23C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597929
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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