A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374968



Internal ID21032521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153998077..154018663hg38UCSC Ensembl
chr3:153715866..153736452hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3820587
hg1920587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374968
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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