A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457816



Internal ID22515697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:24906433..24909132hg38UCSC Ensembl
chr12:25059367..25062066hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853044
Supporting Variants
Samples
Known GenesBCAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457816
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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