A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490465



Internal ID22548388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67172892..67179127hg38UCSC Ensembl
chr4:68038610..68044845hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg386236
hg196236
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840078
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490465
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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