A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961140



Internal ID41403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181143124..181148132hg38UCSC Ensembl
chr4:182064277..182069285hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg385009
hg195009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459379
Supporting Variants
Samples
Known GenesLINC00290
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961140
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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