A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501167



Internal ID22559104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12831331..12837730hg38UCSC Ensembl
chr6:12831563..12837962hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843748
Supporting Variants
Samples
Known GenesPHACTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501167
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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