A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620324



Internal ID21568629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85712024..85712024hg38UCSC Ensembl
chr2:85939147..85939147hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115625
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620324
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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