A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504368



Internal ID22562311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24804297..24806501hg38UCSC Ensembl
chr6:24804525..24806729hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382205
hg192205
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844579
Supporting Variants
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504368
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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