A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610500



Internal ID6997417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117854432..117857596hg38UCSC Ensembl
Innerchr6:117854455..117857574hg38UCSC Ensembl
Outerchr6:117854410..117857619hg38UCSC Ensembl
chr6:118175595..118178759hg19UCSC Ensembl
Innerchr6:118175618..118178737hg19UCSC Ensembl
Outerchr6:118175573..118178782hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg383165
hg193165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12515961
SamplesHG00881
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610500
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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