A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961264



Internal ID41484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186008703..186213068hg38UCSC Ensembl
chr4:186929857..187134222hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38204366
hg19204366
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140977
Supporting Variants
Samples
Known GenesCYP4V2, FAM149A, FLJ38576, TLR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961264
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00203


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