A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357527



Internal ID21015080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67387773..67461789hg38UCSC Ensembl
chr3:67438197..67512213hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3874017
hg1974017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103637
Samples
Known GenesSUCLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357527
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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