A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977723



Internal ID20544763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103098284..103101968hg38UCSC Ensembl
chr10:104858041..104861725hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg383685
hg193685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452355
Supporting Variants
Samples
Known GenesNT5C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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