A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598560



Internal ID6985696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167280104..167293715hg38UCSC Ensembl
Innerchr3:167280104..167293715hg38UCSC Ensembl
Outerchr3:167279604..167294215hg38UCSC Ensembl
chr3:166997892..167011503hg19UCSC Ensembl
Innerchr3:166997892..167011503hg19UCSC Ensembl
Outerchr3:166997392..167012003hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3813612
hg1913612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11218888
SamplesHG01785
Known GenesZBBX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598560
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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