A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912445



Internal ID22687661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68781533..68781842hg38UCSC Ensembl
chr10:70541290..70541599hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349727
Samples
Known GenesCCAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912445
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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