A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11156817



Internal ID3871578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136225298..136239854hg38UCSC Ensembl
Innerchr3:136225319..136239833hg38UCSC Ensembl
Outerchr3:136225277..136239875hg38UCSC Ensembl
chr3:135944140..135958696hg19UCSC Ensembl
Innerchr3:135944161..135958675hg19UCSC Ensembl
Outerchr3:135944119..135958717hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3814557
hg1914557
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597885
Supporting Variants
SamplesHG03515
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11156817
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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