A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456218



Internal ID22514095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118009259..118010379hg38UCSC Ensembl
chr12:118447064..118448184hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853942
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456218
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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