A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460823



Internal ID22518706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8023807..8025386hg38UCSC Ensembl
chr10:8065770..8067349hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381580
hg191580
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460823
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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