A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502424



Internal ID22560364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150604977..150611933hg38UCSC Ensembl
chr6:150926113..150933069hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg386957
hg196957
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844750
Supporting Variants
Samples
Known GenesPLEKHG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502424
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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