A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356865



Internal ID22582534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24422864..24422864hg38UCSC Ensembl
chr10:24711793..24711793hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5953390
Supporting Variants
Samples
Known GenesKIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356865
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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