A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222187



Internal ID20789227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33611576..33650906hg38UCSC Ensembl
chr6:33579353..33618683hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3839331
hg1939331
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403985
Supporting Variants
Samples
Known GenesITPR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222187
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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