A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426364



Internal ID21083917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15272974..15329765hg38UCSC Ensembl
chr9:15272972..15329763hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3856792
hg1956792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175043
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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