A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521224



Internal ID20894585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69421789..69423098hg38UCSC Ensembl
chr17:67417930..67419239hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381310
hg191310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037637
Samples
Known GenesMAP2K6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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