A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578611



Internal ID21527082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214881165..214881225hg38UCSC Ensembl
chr1:215054508..215054568hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062653
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578611
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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