A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441217



Internal ID21098770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18098567..18099301hg38UCSC Ensembl
chr10:18387496..18388230hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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