A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949501



Internal ID22724950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174382772..174382772hg38UCSC Ensembl
chr4:175303923..175303923hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949501
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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