A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497080



Internal ID22555014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167173281..167182779hg38UCSC Ensembl
chr5:166600286..166609784hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg389499
hg199499
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842111
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497080
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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