A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565121



Internal ID21513432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34323264..34323323hg38UCSC Ensembl
chr1:34788865..34788924hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065284
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565121
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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