A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914950



Internal ID22690168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44313195..44315117hg38UCSC Ensembl
chr10:44808643..44810565hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381923
hg191923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914950
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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