A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490159



Internal ID22548081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120759982..120817445hg38UCSC Ensembl
chr4:121681137..121738600hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3857464
hg1957464
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837642
Supporting Variants
Samples
Known GenesPRDM5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490159
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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