A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12631262



Internal ID6709869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166267954..166281187hg38UCSC Ensembl
Innerchr6:166267954..166281187hg38UCSC Ensembl
Outerchr6:166267454..166281687hg38UCSC Ensembl
chr6:166681442..166694675hg19UCSC Ensembl
Innerchr6:166681442..166694675hg19UCSC Ensembl
Outerchr6:166680942..166695175hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3813234
hg1913234
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611632
Supporting Variants
SamplesNA20845
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12631262
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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