A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512722



Internal ID20886059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39949685..39958630hg38UCSC Ensembl
chr17:38105938..38114883hg19UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg388946
hg198946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512722
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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