A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406963



Internal ID21064516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51963956..51964447hg38UCSC Ensembl
chr5:51259790..51260281hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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