A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598413



Internal ID6985549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161630234..161631114hg38UCSC Ensembl
Innerchr3:161630245..161631103hg38UCSC Ensembl
Outerchr3:161630223..161631125hg38UCSC Ensembl
chr3:161348022..161348902hg19UCSC Ensembl
Innerchr3:161348033..161348891hg19UCSC Ensembl
Outerchr3:161348011..161348913hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11200023, essv11200024
SamplesHG03696, HG03848
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598413
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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