A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224129



Internal ID20791169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63291101..63319500hg38UCSC Ensembl
chr9:67246073..67274472hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3828400
hg1928400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446975
Supporting Variants
Samples
Known GenesAQP7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224129
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00133


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