A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908458



Internal ID22683668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38872429..38896006hg38UCSC Ensembl
chr7:38912029..38935606hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3823578
hg1923578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442871
Samples
Known GenesVPS41
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908458
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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