A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285390



Internal ID20494608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113457661..113457817hg38UCSC Ensembl
chr5:112793358..112793514hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737431
Supporting Variants
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285390
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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