A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426484



Internal ID21084037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15302423..15397066hg38UCSC Ensembl
chr9:15302421..15397064hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3894644
hg1994644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7627n223
Supporting Variantsnssv18175639
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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