A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957514



Internal ID38987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139031521..139031582hg38UCSC Ensembl
chr4:139952675..139952736hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462568
Supporting Variants
Samples
Known GenesCCRN4L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957514
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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