A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614614



Internal ID21562919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11346712..11346712hg38UCSC Ensembl
chr2:11486838..11486838hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3811335
hg1911335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17108208
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614614
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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