A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895629



Internal ID22670714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52737378..52742354hg38UCSC Ensembl
chr4:53603545..53608521hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg384977
hg194977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895629
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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