A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325796



Internal ID20858928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52005469..52012595hg38UCSC Ensembl
chr1:52471141..52478267hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg387127
hg197127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325796
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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