A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446860



Internal ID22113037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22029136..22029290hg38UCSC Ensembl
chr7:22068754..22068908hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756434
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446860
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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