A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447222



Internal ID21104775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106370580..106421559hg38UCSC Ensembl
chr9:109132861..109183840hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3850980
hg1950980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172460
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447222
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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