A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611007



Internal ID21559312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94957481..94957481hg38UCSC Ensembl
chr1:95423037..95423037hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067163
SamplesNA20509
Known GenesLOC729970
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611007
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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