A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453716



Internal ID21111269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72906209..73538841hg38UCSC Ensembl
chr9:75521125..76153757hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38632633
hg19632633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225275
Samples
Known GenesALDH1A1, ANXA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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