A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369974



Internal ID21027527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37254875..37270223hg38UCSC Ensembl
chr3:37296366..37311714hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3815349
hg1915349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102140
Samples
Known GenesGOLGA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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