A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617057



Internal ID21565362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11641682..11641682hg38UCSC Ensembl
chr1:11701739..11701739hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060127
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617057
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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