A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526319



Internal ID20899680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78577705..78601584hg38UCSC Ensembl
chr17:76573787..76597666hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3823880
hg1923880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3253n223
Supporting Variantsnssv18177157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526319
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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