A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595495



Internal ID6982813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20972954..20977119hg38UCSC Ensembl
Innerchr3:20972954..20977119hg38UCSC Ensembl
Outerchr3:20972454..20977619hg38UCSC Ensembl
chr3:21014446..21018611hg19UCSC Ensembl
Innerchr3:21014446..21018611hg19UCSC Ensembl
Outerchr3:21013946..21019111hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384166
hg194166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv874e214
Supporting Variantsessv10946441, essv10946443, essv10946444, essv10946442
SamplesNA20531, NA20764, HG01613, HG03694
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595495
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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