A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950739



Internal ID22726135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31203675..31203675hg38UCSC Ensembl
chr4:31205297..31205297hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423457
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950739
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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