A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441696



Internal ID21099249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74762824..74769237hg38UCSC Ensembl
chr10:76522582..76528995hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg386414
hg196414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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