A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636552



Internal ID21584857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142862422..142862422hg38UCSC Ensembl
chr6:143183559..143183559hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143963
SamplesNA19238
Known GenesHIVEP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636552
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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