A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463187



Internal ID22521072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11439554..11449210hg38UCSC Ensembl
chr12:11592488..11602144hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg389657
hg199657
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463187
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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