A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248160



Internal ID21302038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35364451..35370946hg38UCSC Ensembl
Outerchr19:35358591..35375842hg38UCSC Ensembl
Innerchr19:35855353..35861848hg19UCSC Ensembl
Outerchr19:35849493..35866744hg19UCSC Ensembl
Innerchr19:40547193..40553688hg18UCSC Ensembl
Outerchr19:40541333..40558584hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3817252
hg1917252
hg1817252
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169895
Supporting Variants
SamplesMLY_11
Known GenesFFAR3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248160
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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