A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486462



Internal ID22544376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155879766..155886429hg38UCSC Ensembl
chr3:155597555..155604218hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg386664
hg196664
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835010
Supporting Variants
Samples
Known GenesGMPS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486462
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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