A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432777



Internal ID21090330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12278501..12422400hg38UCSC Ensembl
chr9:12278501..12422400hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38143900
hg19143900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7619n223
Supporting Variantsnssv18176504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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