A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059623



Internal ID21470060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102093648..102093648hg38UCSC Ensembl
chr1:102559204..102559204hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617423
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059623
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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