A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441582



Internal ID21099135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128123476..128124374hg38UCSC Ensembl
chr9:130885755..130886653hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38899
hg19899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176858
Samples
Known GenesPTGES2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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