A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534598



Internal ID20907959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76300077..76310244hg38UCSC Ensembl
chr17:74296158..74306325hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3810168
hg1910168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192768
Samples
Known GenesQRICH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer