A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350898



Internal ID22576567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89792325..89792405hg38UCSC Ensembl
chr10:91552082..91552162hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350898
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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