A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630001



Internal ID21578306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61762543..61762543hg38UCSC Ensembl
chr8:62675102..62675102hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153519
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630001
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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