A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451914



Internal ID21109467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132713646..132865371hg38UCSC Ensembl
chr9:135589033..135740758hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38151726
hg19151726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231450
Samples
Known GenesAK8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451914
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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