A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528283



Internal ID20901644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69430096..69435266hg38UCSC Ensembl
chr17:67426237..67431407hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg385171
hg195171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037638
Samples
Known GenesMAP2K6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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