A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543594



Internal ID21867949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139045617..139046670hg38UCSC Ensembl
chr4:139966771..139967824hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995235
Supporting Variants
Samples
Known GenesCCRN4L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543594
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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