A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563136



Internal ID21887491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155267011..155267011hg38UCSC Ensembl
chr5:154646571..154646571hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6069568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563136
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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