A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929304



Internal ID22704555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75231963..75232241hg38UCSC Ensembl
chr16:75265861..75266139hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384019
Samples
Known GenesBCAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929304
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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