A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435846



Internal ID21093399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89449046..89461788hg38UCSC Ensembl
chr9:92063961..92076703hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3812743
hg1912743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193987
Samples
Known GenesSEMA4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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