A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367817



Internal ID22593486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50503411..50503411hg38UCSC Ensembl
chr10:52263171..52263171hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956549
Supporting Variants
Samples
Known GenesSGMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367817
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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