A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572521



Internal ID21520912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60195337..60195523hg38UCSC Ensembl
chr1:60661009..60661195hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065921
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572521
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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