A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461615



Internal ID22519500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181033574..181035226hg38UCSC Ensembl
chr1:181002710..181004362hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381653
hg191653
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828437
Supporting Variants
Samples
Known GenesMR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461615
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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