A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234823



Internal ID20801863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41773601..41907300hg38UCSC Ensembl
chr9:65648662..67670238hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38133700
hg192021577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436008
Supporting Variants
Samples
Known GenesAQP7P1, LOC286297, PTGER4P2-CDK2AP2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234823
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00346


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