A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461066



Internal ID22518949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222509049..222511155hg38UCSC Ensembl
chr1:222682391..222684497hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg382107
hg192107
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829370
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461066
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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