A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361362



Internal ID21018915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99874801..99879200hg38UCSC Ensembl
chr3:99593645..99598044hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211313
Samples
Known GenesCMSS1, FILIP1L, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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