A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206502



Internal ID20773542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113497501..113523200hg38UCSC Ensembl
chr2:114255078..114280777hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3825700
hg1925700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347650
Supporting Variants
Samples
Known GenesFOXD4L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206502
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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