A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523022



Internal ID20896383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69279154..69304260hg38UCSC Ensembl
chr17:67275295..67300401hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3825107
hg1925107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188387
Samples
Known GenesABCA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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