A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636290



Internal ID21584595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:136049948..136049948hg38UCSC Ensembl
chr8:137062191..137062191hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153215
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636290
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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