A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445526



Internal ID22111705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23549706..23550346hg38UCSC Ensembl
chr8:23407219..23407859hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762595
Samples
Known GenesSLC25A37
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445526
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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