A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611702



Internal ID6998608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168956552..168958282hg38UCSC Ensembl
Innerchr6:168956562..168958273hg38UCSC Ensembl
Outerchr6:168956543..168958292hg38UCSC Ensembl
chr6:169356647..169358377hg19UCSC Ensembl
Innerchr6:169356657..169358368hg19UCSC Ensembl
Outerchr6:169356638..169358387hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381731
hg191731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12646407
SamplesHG03476
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611702
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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