A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574086



Internal ID21522498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212185228..212185291hg38UCSC Ensembl
chr1:212358570..212358633hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062303
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574086
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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