A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736436



Internal ID20512385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35925853..35926053hg38UCSC Ensembl
chr20:34513775..34513975hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293998
Samples
Known GenesPHF20
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736436
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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