A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060802



Internal ID21478397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151928005..151928005hg38UCSC Ensembl
chr1:151900481..151900481hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383089
hg193089
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613542
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060802
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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