A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596923



Internal ID6984237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88417756..88422416hg38UCSC Ensembl
Innerchr3:88417791..88422382hg38UCSC Ensembl
Outerchr3:88417722..88422451hg38UCSC Ensembl
chr3:88466906..88471566hg19UCSC Ensembl
Innerchr3:88466941..88471532hg19UCSC Ensembl
Outerchr3:88466872..88471601hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg384661
hg194661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11066273, essv11066272, essv11066270, essv11066271
SamplesHG03370, NA18605, HG03291, HG02283
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596923
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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