A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525786



Internal ID301934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51600874..51607000hg38UCSC Ensembl
chr15:51893071..51899197hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386127
hg196127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702701
Samples
Known GenesDMXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525786
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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