A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322585



Internal ID20855698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184610722..184645531hg38UCSC Ensembl
chr1:184579856..184614665hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3834810
hg1934810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201764
Samples
Known GenesC1orf21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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