A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597825



Internal ID6984963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132328496..132333897hg38UCSC Ensembl
Innerchr3:132328496..132333897hg38UCSC Ensembl
Outerchr3:132328203..132334184hg38UCSC Ensembl
chr3:132047340..132052741hg19UCSC Ensembl
Innerchr3:132047340..132052741hg19UCSC Ensembl
Outerchr3:132047047..132053028hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg385402
hg195402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11154456, essv11154457
SamplesHG00867, HG02371
Known GenesACPP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597825
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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