A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433198



Internal ID211923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39893566..39893617hg38UCSC Ensembl
chr15:40185767..40185818hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701598
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433198
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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