A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511119



Internal ID287715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41810250..41810397hg38UCSC Ensembl
chr15:42102448..42102595hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701162
Samples
Known GenesMAPKBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511119
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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