A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037980



Internal ID21947323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49313712..49335431hg38UCSC Ensembl
chr15:49605909..49627628hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3821720
hg1921720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607631
Samples
Known GenesFAM227B, GALK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037980
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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