A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440597



Internal ID22106775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58410519..58410763hg38UCSC Ensembl
chr19:58921886..58922130hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760924
Samples
Known GenesZNF584
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440597
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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