A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447938



Internal ID21105491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66780670..66911504hg38UCSC Ensembl
chr10:68540428..68671262hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38130835
hg19130835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv790n223
Supporting Variantsnssv17983911
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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