A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980723



Internal ID20547763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13128533..13129363hg38UCSC Ensembl
chr10:13170533..13171363hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38831
hg19831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445714
Supporting Variants
Samples
Known GenesOPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00191


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