A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207440



Internal ID20774481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175243790..175293094hg38UCSC Ensembl
chr2:176108518..176157822hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3849305
hg1949305
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6349222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207440
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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