A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977136



Internal ID20544176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100428549..100444988hg38UCSC Ensembl
chr10:102188306..102204745hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3816440
hg1916440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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