A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520858



Internal ID20894219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77956901..77959800hg38UCSC Ensembl
chr17:75952983..75955882hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3252n223
Supporting Variantsnssv18189814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520858
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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