A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444391



Internal ID21101944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102312477..102349244hg38UCSC Ensembl
chr9:105074759..105111526hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3836768
hg1936768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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