A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499799



Internal ID22557735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42963377..42975116hg38UCSC Ensembl
chr5:42963479..42975218hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3811740
hg1911740
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499799
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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