A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455304



Internal ID21112857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81806344..81808336hg38UCSC Ensembl
chr9:84421259..84423251hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381993
hg191993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455304
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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