A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527906



Internal ID20901267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51264835..51265737hg38UCSC Ensembl
chr17:49342196..49343098hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036848
Samples
Known GenesUTP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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