A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934778



Internal ID22710109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80761051..80763198hg38UCSC Ensembl
chr15:81053392..81055539hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382148
hg192148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934778
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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