A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975850



Internal ID22750785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116987501..116987501hg38UCSC Ensembl
chr10:118747012..118747012hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357853
Samples
Known GenesKIAA1598
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975850
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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