A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645996



Internal ID7032742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48528501..48529177hg38UCSC Ensembl
Innerchr20:48528504..48529174hg38UCSC Ensembl
Outerchr20:48528498..48529180hg38UCSC Ensembl
chr20:47145039..47145715hg19UCSC Ensembl
Innerchr20:47145042..47145712hg19UCSC Ensembl
Outerchr20:47145036..47145718hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16198251
SamplesHG02774
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645996
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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