A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436861



Internal ID21094414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109524500..109643083hg38UCSC Ensembl
chr10:111284258..111402841hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38118584
hg19118584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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