A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021999



Internal ID21931342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39919443..39919503hg38UCSC Ensembl
chr15:40211644..40211704hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609044
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021999
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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