A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983041



Internal ID20550081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68725207..68728029hg38UCSC Ensembl
chr10:70484964..70487786hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382823
hg192823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444544
Supporting Variants
Samples
Known GenesCCAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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