A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432758



Internal ID21090311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15296001..15304000hg38UCSC Ensembl
chr9:15295999..15303998hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175636
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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