A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439827



Internal ID21097380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17726622..17733972hg38UCSC Ensembl
chr10:17768621..17775971hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg387351
hg197351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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