A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951370



Internal ID34937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:60413685..60495138hg38UCSC Ensembl
chr4:61279403..61360856hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3881454
hg1981454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141247
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951370
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000782


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