A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983820



Internal ID20550860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72601314..72603399hg38UCSC Ensembl
chr10:74361072..74363157hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382086
hg192086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445775
Supporting Variants
Samples
Known GenesMICU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983820
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer