A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645797



Internal ID6685858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38949708..38974834hg38UCSC Ensembl
chr20:37578351..37603477hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3825127
hg1925127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16182086
SamplesHG01816
Known GenesDHX35, FAM83D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645797
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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