A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598791



Internal ID6985926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177289419..177296046hg38UCSC Ensembl
Innerchr3:177289419..177296046hg38UCSC Ensembl
Outerchr3:177288919..177296546hg38UCSC Ensembl
chr3:177007207..177013834hg19UCSC Ensembl
Innerchr3:177007207..177013834hg19UCSC Ensembl
Outerchr3:177006707..177014334hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg386628
hg196628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11237577, essv11237576
SamplesHG02820, HG01509
Known GenesLINC00501
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598791
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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