A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496732



Internal ID22554666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43541203..43542908hg38UCSC Ensembl
chr5:43541305..43543010hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg381706
hg191706
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842995
Supporting Variants
Samples
Known GenesPAIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496732
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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