A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525411



Internal ID20898772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62017935..62029045hg38UCSC Ensembl
chr17:60095296..60106406hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3811111
hg1911111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037147
Samples
Known GenesMED13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525411
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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