A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474034



Internal ID22531928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82055559..82064600hg38UCSC Ensembl
chr16:82089164..82098205hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg389042
hg199042
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884457
Supporting Variants
Samples
Known GenesHSD17B2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474034
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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