A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430352



Internal ID21087905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15006946..15152017hg38UCSC Ensembl
chr9:15006944..15152015hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38145072
hg19145072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7626n223
Supporting Variantsnssv18175017
Samples
Known GenesLOC389705
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430352
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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