A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621259



Internal ID21813306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58500688..58500688hg38UCSC Ensembl
chr17:56578049..56578049hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089921
Supporting Variants
Samples
Known GenesMTMR4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621259
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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