A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562811



Internal ID21887166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173726878..173726878hg38UCSC Ensembl
chr5:173153881..173153881hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076537
Supporting Variants
Samples
Known GenesLOC101928136
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562811
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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