A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358227



Internal ID21015780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28217828..28252835hg38UCSC Ensembl
chr3:28259319..28294326hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3835008
hg1935008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101974
Samples
Known GenesCMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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