A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445239



Internal ID21102792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96383301..96384000hg38UCSC Ensembl
chr9:99145583..99146282hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190205
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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