A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981373



Internal ID20548413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29853988..29854603hg38UCSC Ensembl
chr10:30142917..30143532hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981373
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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