A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423625



Internal ID21081178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6412201..6413900hg38UCSC Ensembl
chr9:6412201..6413900hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224976
Samples
Known GenesUHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423625
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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