A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978939



Internal ID20545979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16763315..16870932hg38UCSC Ensembl
chr10:16805314..16912931hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38107618
hg19107618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448456
Supporting Variants
Samples
Known GenesCUBN, RSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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