A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598794



Internal ID6985929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177314783..177320261hg38UCSC Ensembl
Innerchr3:177314833..177320211hg38UCSC Ensembl
Outerchr3:177314709..177320335hg38UCSC Ensembl
chr3:177032571..177038049hg19UCSC Ensembl
Innerchr3:177032621..177037999hg19UCSC Ensembl
Outerchr3:177032497..177038123hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg385479
hg195479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11237590, essv11237591
SamplesNA19072, HG01951
Known GenesLINC00501
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598794
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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