A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983061



Internal ID20550101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69097343..69097733hg38UCSC Ensembl
chr10:70857099..70857489hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438341
Supporting Variants
Samples
Known GenesSRGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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