A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555204



Internal ID21879559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121472459..122035370hg38UCSC Ensembl
chr5:120808154..121371065hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38562912
hg19562912
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001189
Supporting Variants
Samples
Known GenesFTMT, SRFBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555204
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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