A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371206



Internal ID22596875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69392020..69392020hg38UCSC Ensembl
chr1:69857703..69857703hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955347
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371206
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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