A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608098



Internal ID6995028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11634686..11641031hg38UCSC Ensembl
Innerchr6:11634732..11640985hg38UCSC Ensembl
Outerchr6:11634640..11641077hg38UCSC Ensembl
chr6:11634919..11641264hg19UCSC Ensembl
Innerchr6:11634965..11641218hg19UCSC Ensembl
Outerchr6:11634873..11641310hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg386346
hg196346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12189408, essv12189409
SamplesHG00157, HG00357
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608098
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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