A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448879



Internal ID22115057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4420273..4420327hg38UCSC Ensembl
chr1:4480333..4480387hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764592
Samples
Known GenesLOC284661
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448879
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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