A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469311



Internal ID22527202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75043465..75048281hg38UCSC Ensembl
chr10:76803223..76808039hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg384817
hg194817
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858018
Supporting Variants
Samples
Known GenesDUPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469311
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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