A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522980



Internal ID20896341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81605024..81605375hg38UCSC Ensembl
chr17:79572050..79572401hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039185
Samples
Known GenesNPLOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522980
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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