A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961032



Internal ID41329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173342372..173342753hg38UCSC Ensembl
chr4:174263523..174263904hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141356
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961032
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005153


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