A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429776



Internal ID21087329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11731169..12228059hg38UCSC Ensembl
chr9:11731169..12228059hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38496891
hg19496891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7575n223
Supporting Variantsnssv18173888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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