A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631250



Internal ID21579555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160475012..160475012hg38UCSC Ensembl
chr5:159902019..159902019hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121143
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631250
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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