A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441222



Internal ID21098775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68608521..68609586hg38UCSC Ensembl
chr10:70368278..70369343hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381066
hg191066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983033
Samples
Known GenesTET1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441222
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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