A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564072



Internal ID336994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42194628..42248498hg38UCSC Ensembl
chr15:42486826..42540696hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3853871
hg1953871
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699769
Samples
Known GenesMIR627, TMEM87A, VPS39
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5564072
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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