A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950624



Internal ID22726019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97647775..97647775hg38UCSC Ensembl
chr10:99407532..99407532hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361384
Samples
Known GenesPI4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950624
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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