A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929916



Internal ID22705175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52125936..52126802hg38UCSC Ensembl
chr15:52418133..52418999hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378984
Samples
Known GenesGNB5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929916
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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