A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506494



Internal ID22564442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52902124..52922345hg38UCSC Ensembl
chr6:52766922..52787143hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3820222
hg1920222
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845546
Supporting Variants
Samples
Known GenesGSTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506494
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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