A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469000



Internal ID22526890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11423373..11434978hg38UCSC Ensembl
chr12:11576307..11587912hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3811606
hg1911606
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469000
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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