A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10961158



Internal ID5918749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27597537..27611036hg38UCSC Ensembl
Innerchr3:27597555..27611019hg38UCSC Ensembl
Outerchr3:27597520..27611054hg38UCSC Ensembl
chr3:27639028..27652527hg19UCSC Ensembl
Innerchr3:27639046..27652510hg19UCSC Ensembl
Outerchr3:27639011..27652545hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3813500
hg1913500
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595670
Supporting Variants
SamplesNA19328
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10961158
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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