A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918514



Internal ID22693735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97725138..97734591hg38UCSC Ensembl
chr10:99484895..99494348hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg389454
hg199454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918514
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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