A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440558



Internal ID22106736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41277590..41278770hg38UCSC Ensembl
chr20:39906230..39907410hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761094
Samples
Known GenesZHX3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440558
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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