A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423880



Internal ID202888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90987684..90987742hg38UCSC Ensembl
chr1:91453241..91453299hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905950
Samples
Known GenesZNF644
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423880
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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