A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466908



Internal ID22524799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19816355..19820372hg38UCSC Ensembl
chr12:19969289..19973306hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg384018
hg194018
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851449
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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