A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439012



Internal ID21096565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117195447..117196177hg38UCSC Ensembl
chr9:119957726..119958456hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173881
Samples
Known GenesASTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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