A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364571



Internal ID22590240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72483557..72491396hg38UCSC Ensembl
chr10:74243315..74251154hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg387840
hg197840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908015
Supporting Variants
Samples
Known GenesMICU1, MIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364571
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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