A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645796



Internal ID6685857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38949708..38974834hg38UCSC Ensembl
chr20:37578351..37603477hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3825127
hg1925127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16182085
SamplesNA19377
Known GenesDHX35, FAM83D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645796
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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