A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645732



Internal ID6685793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36256528..36266639hg38UCSC Ensembl
Innerchr20:36256528..36266639hg38UCSC Ensembl
Outerchr20:36256487..36266664hg38UCSC Ensembl
chr20:34844450..34854561hg19UCSC Ensembl
Innerchr20:34844450..34854561hg19UCSC Ensembl
Outerchr20:34844409..34854586hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3810112
hg1910112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16179777
SamplesNA19676
Known GenesAAR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645732
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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