A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356040



Internal ID21013593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180663854..180689924hg38UCSC Ensembl
chr3:180381642..180407712hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3826071
hg1926071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100490
Samples
Known GenesCCDC39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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