A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977739



Internal ID20544779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104210417..104210803hg38UCSC Ensembl
chr10:105970175..105970561hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438481
Supporting Variants
Samples
Known GenesWDR96
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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