A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416488



Internal ID22474358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173114443..173114443hg38UCSC Ensembl
chr4:174035594..174035594hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965043
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416488
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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