A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646032



Internal ID7032777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49779913..49782141hg38UCSC Ensembl
Innerchr20:49779921..49782133hg38UCSC Ensembl
Outerchr20:49779905..49782149hg38UCSC Ensembl
chr20:48396450..48398678hg19UCSC Ensembl
Innerchr20:48396458..48398670hg19UCSC Ensembl
Outerchr20:48396442..48398686hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg382229
hg192229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16198936, essv16198935, essv16198938, essv16198934, essv16198937
SamplesHG03593, HG03607, HG02736, HG03755, HG03653
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646032
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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