A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441511



Internal ID21099064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127527945..127529665hg38UCSC Ensembl
chr9:130290224..130291944hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381721
hg191721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176808
Samples
Known GenesFAM129B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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