A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433575



Internal ID21091128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6413601..6419200hg38UCSC Ensembl
chr9:6413601..6419200hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232285
Samples
Known GenesUHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433575
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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