A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062035



Internal ID21505594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19491045..19491045hg38UCSC Ensembl
chr1:19817539..19817539hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604623
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062035
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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