A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11237591



Internal ID5661842
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598794
Supporting Variants
SamplesNA19072
Known GenesLINC00501
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11237591
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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