A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598289



Internal ID6638554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155933984..156058489hg38UCSC Ensembl
Innerchr3:155933984..156058489hg38UCSC Ensembl
Outerchr3:155933484..156058989hg38UCSC Ensembl
chr3:155651773..155776278hg19UCSC Ensembl
Innerchr3:155651773..155776278hg19UCSC Ensembl
Outerchr3:155651273..155776778hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38124506
hg19124506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11191924
SamplesNA21088
Known GenesGMPS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598289
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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