A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633903



Internal ID21582208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:71675814..71675814hg38UCSC Ensembl
chr8:72588049..72588049hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142401
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633903
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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