A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449765



Internal ID21107318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86253826..86254934hg38UCSC Ensembl
chr9:88868741..88869849hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381109
hg191109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186071
Samples
Known GenesC9orf153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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