A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617856



Internal ID21566161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195536632..195536632hg38UCSC Ensembl
chr2:196401356..196401356hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109927
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617856
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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