A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594178



Internal ID20967249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51170256..51170526hg38UCSC Ensembl
chr17:49247617..49247887hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245207
Samples
Known GenesNME1-NME2, NME2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594178
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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