A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444000



Internal ID21101553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97281363..97283994hg38UCSC Ensembl
chr9:100043645..100046276hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382632
hg192632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186999
Samples
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444000
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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