A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456776



Internal ID22514655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:79562491..79565640hg38UCSC Ensembl
chr12:79956271..79959420hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg383150
hg193150
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456776
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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