A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366657



Internal ID22592326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122644200..122644200hg38UCSC Ensembl
chr10:124403716..124403716hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366657
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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