A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208977



Internal ID20776017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132811040..132821970hg38UCSC Ensembl
chr3:132529884..132540814hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3810931
hg1910931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355968
Supporting Variants
Samples
Known GenesNPHP3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208977
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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