A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895639



Internal ID22670724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:93126436..93190682hg38UCSC Ensembl
chr4:94047587..94111833hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg3864247
hg1964247
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411320
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895639
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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