A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441136



Internal ID22107316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63879560..63879680hg38UCSC Ensembl
chr20:62510913..62511033hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763071
Samples
Known GenesTPD52L2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441136
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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