A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004945



Internal ID21914288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68761542..68764697hg38UCSC Ensembl
chr10:70521299..70524454hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383156
hg193156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591152
Samples
Known GenesCCAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004945
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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