A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977983



Internal ID20545023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115535061..115586235hg38UCSC Ensembl
chr10:117294571..117345745hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3851175
hg1951175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444414
Supporting Variants
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00014


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