A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635009



Internal ID21583314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61600616..61600616hg38UCSC Ensembl
chr5:60896443..60896443hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144043
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635009
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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