A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938052



Internal ID22713429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41320934..41321091hg38UCSC Ensembl
chr15:41613132..41613289hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379202
Samples
Known GenesOIP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938052
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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