A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521222



Internal ID20894583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78303255..78308885hg38UCSC Ensembl
chr17:76299336..76304966hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg385631
hg195631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521222
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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