A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605816



Internal ID21554121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91641220..91641220hg38UCSC Ensembl
chr1:92106777..92106777hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067133
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605816
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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