A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363280



Internal ID21020833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97844357..97999939hg38UCSC Ensembl
chr3:97563201..97718783hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38155583
hg19155583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211278
Samples
Known GenesCRYBG3, GABRR3, MINA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363280
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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