A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916980



Internal ID22692199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43563387..43564572hg38UCSC Ensembl
chr10:44058835..44060020hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381186
hg191186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367363
Samples
Known GenesZNF239
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916980
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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