A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526273



Internal ID20899634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59547749..59549136hg38UCSC Ensembl
chr17:57625110..57626497hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg381388
hg191388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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