A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451928



Internal ID22509800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31995679..32000047hg38UCSC Ensembl
chr12:32148613..32152981hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg384369
hg194369
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451928
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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