A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642888



Internal ID21591193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6830777..6830777hg38UCSC Ensembl
chr5:6830890..6830890hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148397
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642888
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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