A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448920



Internal ID22115098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70611881..70612015hg38UCSC Ensembl
chr14:71078598..71078732hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758640
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448920
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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