A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062807



Internal ID21463658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222376903..222377773hg38UCSC Ensembl
chr1:222550245..222551115hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578832
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062807
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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