A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331531



Internal ID20864695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21178473..21187106hg38UCSC Ensembl
chr1:21504966..21513599hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg388634
hg198634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331531
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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