A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446878



Internal ID21104431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64752701..64754300hg38UCSC Ensembl
chr10:66512458..66514057hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446878
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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