A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439680



Internal ID22105857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91209445..91209784hg38UCSC Ensembl
chr10:92969202..92969541hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762471
Samples
Known GenesPCGF5
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439680
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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