A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433974



Internal ID21091527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11456925..11632345hg38UCSC Ensembl
chr9:11456925..11632345hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38175421
hg19175421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7568n223
Supporting Variantsnssv18175064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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