A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645775



Internal ID6685836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38264344..38392152hg38UCSC Ensembl
chr20:36892746..37020794hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38127809
hg19128049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16180421, essv16180422
SamplesHG03619, NA19454
Known GenesBPI, LBP, LOC149684
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645775
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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