A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439273



Internal ID21096826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121009101..121029100hg38UCSC Ensembl
chr10:122768614..122788613hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3820000
hg1920000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv903n223
Supporting Variantsnssv17980520
Samples
Known GenesMIR5694
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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