A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906048



Internal ID22681242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65758204..65909608hg38UCSC Ensembl
chr6:66468097..66619501hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38151405
hg19151405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448855
Samples
Known GenesSLC25A51P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906048
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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