A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15212077



Internal ID5213893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35160879..35171099hg38UCSC Ensembl
Innerchr15:35160883..35171095hg38UCSC Ensembl
Outerchr15:35160875..35171103hg38UCSC Ensembl
chr15:35453080..35463300hg19UCSC Ensembl
Innerchr15:35453084..35463296hg19UCSC Ensembl
Outerchr15:35453076..35463304hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3810221
hg1910221
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636129
Supporting Variants
SamplesHG00113
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15212077
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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