A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979569



Internal ID20546609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118555632..118556266hg38UCSC Ensembl
chr10:120315144..120315778hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453655
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00047


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