A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060780



Internal ID21501619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150781394..150781394hg38UCSC Ensembl
chr1:150753870..150753870hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611712
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060780
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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