A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372454



Internal ID21030007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37792358..37793254hg38UCSC Ensembl
chr3:37833849..37834745hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102163
Samples
Known GenesITGA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372454
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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