A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359323



Internal ID22584992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87123023..87123152hg38UCSC Ensembl
chr10:88882780..88882909hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920530
Supporting Variants
Samples
Known GenesFAM35A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359323
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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