A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978099



Internal ID20545139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112003986..112004404hg38UCSC Ensembl
chr10:113763744..113764162hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00069


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