A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527668



Internal ID20901029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70795947..70818447hg38UCSC Ensembl
chr17:68792088..68814588hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3822501
hg1922501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527668
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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