A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447609



Internal ID21105162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128278254..128289656hg38UCSC Ensembl
chr9:131040533..131051935hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3811403
hg1911403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176865
Samples
Known GenesSWI5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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