A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445052



Internal ID22111232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171998618..171998737hg38UCSC Ensembl
chr3:171716408..171716527hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765261
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445052
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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