A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978881



Internal ID20545921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128890284..128895550hg38UCSC Ensembl
chr10:130688548..130693814hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385267
hg195267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448492
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978881
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00046


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