A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063359



Internal ID21469489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238293258..238293258hg38UCSC Ensembl
chr1:238456558..238456558hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621611
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063359
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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