A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527721



Internal ID20901082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47001995..47002646hg38UCSC Ensembl
chr17:45079361..45080012hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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