A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500865



Internal ID22558802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106559408..106560757hg38UCSC Ensembl
chr6:107007283..107008632hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843970
Supporting Variants
Samples
Known GenesAIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500865
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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