A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459730



Internal ID22517616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90807433..90809694hg38UCSC Ensembl
chr12:91201210..91203471hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg382262
hg192262
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459730
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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