A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16179972



Internal ID6181788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37157116..37174847hg38UCSC Ensembl
chr20:35785519..35803250hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3817732
hg1917732
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645754
Supporting Variants
SamplesHG00277
Known GenesMROH8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16179972
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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