A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621611



Internal ID21569916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238293258..238293258hg38UCSC Ensembl
chr1:238456558..238456558hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063359
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621611
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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