A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468294



Internal ID22526183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96957371..96959370hg38UCSC Ensembl
chr12:97351149..97353148hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468294
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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