A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522692



Internal ID20896053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66776363..66784720hg38UCSC Ensembl
chr17:64772481..64780838hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg388358
hg198358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037356
Samples
Known GenesPRKCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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