A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978062



Internal ID20545102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111499901..111501200hg38UCSC Ensembl
chr10:113259659..113260958hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00062


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