A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971347



Internal ID48242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90702017..90702026hg38UCSC Ensembl
chr5:89997834..89997843hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553307
Supporting Variants
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971347
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.176165


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