A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593815



Internal ID21542406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73716116..73716343hg38UCSC Ensembl
chr10:75475874..75476101hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071637
SamplesNA12329
Known GenesBMS1P4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593815
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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