A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12585030



Internal ID2586846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151984276..151985418hg38UCSC Ensembl
Innerchr6:151984321..151985374hg38UCSC Ensembl
Outerchr6:151984232..151985463hg38UCSC Ensembl
chr6:152305411..152306553hg19UCSC Ensembl
Innerchr6:152305456..152306509hg19UCSC Ensembl
Outerchr6:152305367..152306598hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611277
Supporting Variants
SamplesNA18571
Known GenesESR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12585030
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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