A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214836



Internal ID20781876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65924801..65951000hg38UCSC Ensembl
chr5:65220629..65246828hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3826200
hg1926200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401993
Supporting Variants
Samples
Known GenesERBB2IP, LOC100303749
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214836
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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