A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455310



Internal ID21112863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100140323..100145714hg38UCSC Ensembl
chr9:102902605..102907996hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385392
hg195392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171533
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455310
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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