A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137833



Internal ID21469681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171240133..171240133hg38UCSC Ensembl
chr5:170667137..170667137hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642045
Supporting Variants
SamplesHG03125
Known GenesRANBP17
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137833
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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