A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062800



Internal ID21483333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21841694..21841694hg38UCSC Ensembl
chr1:22168187..22168187hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615624
Supporting Variants
SamplesHG03732
Known GenesHSPG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062800
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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