A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575589



Internal ID21524018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161007090..161007287hg38UCSC Ensembl
chr1:160976880..160977077hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061242
SamplesHG02818
Known GenesF11R
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575589
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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