A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978117



Internal ID20545157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112374639..112381435hg38UCSC Ensembl
chr10:114134397..114141193hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg386797
hg196797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436302
Supporting Variants
Samples
Known GenesACSL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978117
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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