A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565174



Internal ID21513485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234566983..234573592hg38UCSC Ensembl
chr1:234702729..234709338hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg386610
hg196610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063303
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565174
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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