A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438710



Internal ID21096263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62821301..62922700hg38UCSC Ensembl
chr9:66477125..66578524hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38101400
hg19101400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224142
Samples
Known GenesPTGER4P2-CDK2AP2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438710
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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