A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326531



Internal ID20859667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153453481..153475494hg38UCSC Ensembl
chr1:153425957..153447970hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3822014
hg1922014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200473
Samples
Known GenesS100A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326531
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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