A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519390



Internal ID20892751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76908386..76913433hg38UCSC Ensembl
chr17:74904468..74909515hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg385048
hg195048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037710
Samples
Known GenesMGAT5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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