A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933077



Internal ID22708385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41533190..41533553hg38UCSC Ensembl
chr15:41825388..41825751hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380429
Samples
Known GenesRPAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933077
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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