A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360545



Internal ID22586214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11885322..11885516hg38UCSC Ensembl
chr10:11927321..11927515hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912155
Supporting Variants
Samples
Known GenesPROSER2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360545
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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