A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11156821



Internal ID1158637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136253462..136254638hg38UCSC Ensembl
Innerchr3:136253462..136254638hg38UCSC Ensembl
Outerchr3:136253192..136254915hg38UCSC Ensembl
chr3:135972304..135973480hg19UCSC Ensembl
Innerchr3:135972304..135973480hg19UCSC Ensembl
Outerchr3:135972034..135973757hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381177
hg191177
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597886
Supporting Variants
SamplesHG00188
Known GenesPCCB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11156821
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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