A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608184



Internal ID6995114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15761550..15775161hg38UCSC Ensembl
Innerchr6:15761550..15775161hg38UCSC Ensembl
Outerchr6:15761050..15775661hg38UCSC Ensembl
chr6:15761781..15775392hg19UCSC Ensembl
Innerchr6:15761781..15775392hg19UCSC Ensembl
Outerchr6:15761281..15775892hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3813612
hg1913612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12200597, essv12200600, essv12200599, essv12200598
SamplesNA19393, HG02325, HG02439, HG02014
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608184
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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