A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598872



Internal ID6972390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180557838..180561469hg38UCSC Ensembl
Innerchr3:180557988..180561319hg38UCSC Ensembl
Outerchr3:180557688..180561619hg38UCSC Ensembl
chr3:180275626..180279257hg19UCSC Ensembl
Innerchr3:180275776..180279107hg19UCSC Ensembl
Outerchr3:180275476..180279407hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg383632
hg193632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11250018
SamplesHG02681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598872
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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