A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454893



Internal ID22512770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11462239..11472572hg38UCSC Ensembl
chr12:11615173..11625506hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3810334
hg1910334
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855291
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454893
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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