A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977879



Internal ID20544919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114364935..114368587hg38UCSC Ensembl
chr10:116124694..116128346hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383653
hg193653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450754
Supporting Variants
Samples
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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