A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632044



Internal ID21580349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158429348..158429348hg38UCSC Ensembl
chr5:157856356..157856356hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122032
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632044
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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