A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500150



Internal ID22558087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98342301..98345536hg38UCSC Ensembl
chr5:97678005..97681240hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383236
hg193236
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500150
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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