A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211234



Internal ID20778274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95664690..95669906hg38UCSC Ensembl
chr3:95383534..95388750hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg385217
hg195217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356509
Supporting Variants
Samples
Known GenesMTHFD2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211234
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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