A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356452



Internal ID22582121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100374012..100381214hg38UCSC Ensembl
chr10:102133769..102140971hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg387203
hg197203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909128
Supporting Variants
Samples
Known GenesLINC00263
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356452
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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