A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634625



Internal ID21582930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69204051..69204051hg38UCSC Ensembl
chr5:68499878..68499878hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145915, nssv17152827
SamplesHG03486, HG00512
Known GenesCENPH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634625
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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