A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364945



Internal ID21022498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185453868..185804751hg38UCSC Ensembl
chr3:185171656..185522539hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38350884
hg19350884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212185
Samples
Known GenesC3orf65, IGF2BP2, LIPH, MAP3K13, SENP2, TMEM41A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364945
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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