A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598665



Internal ID6985801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172413597..172422854hg38UCSC Ensembl
Innerchr3:172413637..172422815hg38UCSC Ensembl
Outerchr3:172413558..172422894hg38UCSC Ensembl
chr3:172131387..172140644hg19UCSC Ensembl
Innerchr3:172131427..172140605hg19UCSC Ensembl
Outerchr3:172131348..172140684hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg389258
hg199258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11227295
SamplesHG02019
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598665
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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