A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359957



Internal ID22585626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113539811..113539811hg38UCSC Ensembl
chr10:115299570..115299570hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359957
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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