A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438903



Internal ID217453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9664808..10441581hg38UCSC Ensembl
chr4:9666432..10443205hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38776774
hg19776774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947687
Samples
Known GenesDRD5, MIR3138, SLC2A9, WDR1, ZNF518B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438903
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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