A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448070



Internal ID21105623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68349700..68350264hg38UCSC Ensembl
chr10:70109457..70110021hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983013
Samples
Known GenesRUFY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448070
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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