A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444826



Internal ID21102379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121008901..121028000hg38UCSC Ensembl
chr10:122768414..122787513hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3819100
hg1919100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv903n223
Supporting Variantsnssv17980518
Samples
Known GenesMIR5694
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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