A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208295



Internal ID20775335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201641140..201661114hg38UCSC Ensembl
chr2:202505863..202525837hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3819975
hg1919975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341741
Supporting Variants
Samples
Known GenesMPP4, TMEM237
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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