A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358276



Internal ID21015829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42584990..42588657hg38UCSC Ensembl
chr3:42626482..42630149hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383668
hg193668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099912
Samples
Known GenesSEC22C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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