A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11187542



Internal ID1773416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152155188..152157720hg38UCSC Ensembl
Innerchr3:152155208..152157701hg38UCSC Ensembl
Outerchr3:152155169..152157740hg38UCSC Ensembl
chr3:151872977..151875509hg19UCSC Ensembl
Innerchr3:151872997..151875490hg19UCSC Ensembl
Outerchr3:151872958..151875529hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382533
hg192533
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598200
Supporting Variants
SamplesHG01630
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11187542
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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