A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621874



Internal ID21570179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184410627..184410627hg38UCSC Ensembl
chr1:184379761..184379761hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061452
SamplesNA19238
Known GenesC1orf21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621874
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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