A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360864



Internal ID22586533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119214577..119214636hg38UCSC Ensembl
chr10:120974089..120974148hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908135
Supporting Variants
Samples
Known GenesGRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360864
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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