A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761470



Internal ID22095967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207609754..207612056hg38UCSC Ensembl
chr2:208474478..208476780hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg382303
hg192303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4444763
Supporting Variants
Samples
Known GenesMETTL21A
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761470
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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