A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11187812



Internal ID3281925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152590622..152599608hg38UCSC Ensembl
Innerchr3:152590642..152599589hg38UCSC Ensembl
Outerchr3:152590603..152599628hg38UCSC Ensembl
chr3:152308411..152317397hg19UCSC Ensembl
Innerchr3:152308431..152317378hg19UCSC Ensembl
Outerchr3:152308392..152317417hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg388987
hg198987
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598210
Supporting Variants
SamplesHG02895
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11187812
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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