A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473199



Internal ID22531091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12905625..12910411hg38UCSC Ensembl
chr19:13016439..13021225hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384787
hg194787
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870937
Supporting Variants
Samples
Known GenesSYCE2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473199
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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