A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961171



Internal ID41426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181975578..181975731hg38UCSC Ensembl
chr4:182896731..182896884hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458153
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961171
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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