A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061136



Internal ID21432382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150506578..150506578hg38UCSC Ensembl
chr1:150479054..150479054hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606084
Supporting Variants
SamplesHG00731
Known GenesTARS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061136
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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