A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454810



Internal ID21112363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114673265..114726961hg38UCSC Ensembl
chr9:117435545..117489241hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3853697
hg1953697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175073
Samples
Known GenesLOC100505478
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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