A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363811



Internal ID22589480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91384445..91384445hg38UCSC Ensembl
chr10:93144202..93144202hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960976
Supporting Variants
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363811
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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