A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12180891



Internal ID6069788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5965429..5966562hg38UCSC Ensembl
Innerchr6:5965457..5966534hg38UCSC Ensembl
Outerchr6:5965401..5966590hg38UCSC Ensembl
chr6:5965662..5966795hg19UCSC Ensembl
Innerchr6:5965690..5966767hg19UCSC Ensembl
Outerchr6:5965634..5966823hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381134
hg191134
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3607987
Supporting Variants
SamplesNA19457
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12180891
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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