A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065537



Internal ID21452501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4785747..4785747hg38UCSC Ensembl
chr1:4845807..4845807hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381497
hg191497
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620987
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065537
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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