A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511402



Internal ID20884729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40538288..40541385hg38UCSC Ensembl
chr17:38694540..38697637hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg383098
hg193098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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