A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923150



Internal ID22698376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113494853..113494990hg38UCSC Ensembl
chr10:115254612..115254749hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923150
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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