A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981157



Internal ID20548197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26213129..26216518hg38UCSC Ensembl
chr10:26502058..26505447hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383390
hg193390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436145
Supporting Variants
Samples
Known GenesGAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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