A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373068



Internal ID22598737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62447169..62462823hg38UCSC Ensembl
chr17:60524530..60540184hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3815655
hg1915655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938015
Supporting Variants
Samples
Known GenesMETTL2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373068
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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