A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954037



Internal ID36691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118000076..118000187hg38UCSC Ensembl
chr4:118921231..118921342hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467123
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954037
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003434


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