A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11158566



Internal ID2726122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137395905..137397903hg38UCSC Ensembl
Innerchr3:137395945..137397864hg38UCSC Ensembl
Outerchr3:137395866..137397943hg38UCSC Ensembl
chr3:137114747..137116745hg19UCSC Ensembl
Innerchr3:137114787..137116706hg19UCSC Ensembl
Outerchr3:137114708..137116785hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381999
hg191999
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597900
Supporting Variants
SamplesHG02398
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11158566
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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