A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517068



Internal ID293499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56155749..56156712hg38UCSC Ensembl
chr15:56447947..56448910hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699844
Samples
Known GenesRFX7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517068
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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