A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595492



Internal ID6982810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20937737..20953947hg38UCSC Ensembl
Innerchr3:20937757..20953928hg38UCSC Ensembl
Outerchr3:20937718..20953967hg38UCSC Ensembl
chr3:20979229..20995439hg19UCSC Ensembl
Innerchr3:20979249..20995420hg19UCSC Ensembl
Outerchr3:20979210..20995459hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3816211
hg1916211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10946141, essv10946142, essv10946140, essv10946143
SamplesHG03607, NA18641, NA18988, HG00662
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595492
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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