A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366940



Internal ID22592609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170154653..170159123hg38UCSC Ensembl
chr1:170123794..170128264hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg384471
hg194471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880341
Supporting Variants
Samples
Known GenesMETTL11B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366940
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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