A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931413



Internal ID22706696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74798954..74799031hg38UCSC Ensembl
chr15:75091295..75091372hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379599
Samples
Known GenesCSK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931413
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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