A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533093



Internal ID20906454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64225023..64227271hg38UCSC Ensembl
chr17:62302383..62304631hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg382249
hg192249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037759
Samples
Known GenesTEX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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