A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940121



Internal ID27459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158651434..158651519hg38UCSC Ensembl
chr3:158369223..158369308hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453361
Supporting Variants
Samples
Known GenesGFM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940121
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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