A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936538



Internal ID22711894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70555585..70556633hg38UCSC Ensembl
chr15:70847924..70848972hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936538
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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