A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473246



Internal ID22531138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15022741..15029240hg38UCSC Ensembl
chr19:15133553..15140051hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg386500
hg196499
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882504
Supporting Variants
Samples
Known GenesCCDC105
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473246
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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