A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449469



Internal ID21107022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88940990..88977626hg38UCSC Ensembl
chr9:91555905..91592541hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3836637
hg1936637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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