A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497726



Internal ID22555660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174416397..174419277hg38UCSC Ensembl
chr5:173843400..173846280hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg382881
hg192881
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841587
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497726
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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