A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574916



Internal ID21523339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18982107..18982168hg38UCSC Ensembl
chr1:19308601..19308662hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062144
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574916
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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