A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11173072



Internal ID4041301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146344129..146351017hg38UCSC Ensembl
Innerchr3:146344147..146350999hg38UCSC Ensembl
Outerchr3:146344111..146351035hg38UCSC Ensembl
chr3:146061916..146068804hg19UCSC Ensembl
Innerchr3:146061934..146068786hg19UCSC Ensembl
Outerchr3:146061898..146068822hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg386889
hg196889
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598092
Supporting Variants
SamplesHG03689
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11173072
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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