A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629015



Internal ID21577320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60667360..60667360hg38UCSC Ensembl
chr5:59963187..59963187hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151557
SamplesHG02587
Known GenesDEPDC1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629015
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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