A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439921



Internal ID22106098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38507873..38507939hg38UCSC Ensembl
chr8:38365391..38365457hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766475
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439921
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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