A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950122



Internal ID34101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56091236..56121502hg38UCSC Ensembl
chr4:56957402..56987668hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3830267
hg1930267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950122
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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