A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982752



Internal ID20549792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61220301..61221100hg38UCSC Ensembl
chr10:62980059..62980858hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450453
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982752
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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