A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506416



Internal ID20879695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48147501..48148300hg38UCSC Ensembl
chr15:48439698..48440497hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024712
Samples
Known GenesMYEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506416
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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