A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246845



Internal ID21309098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35364451..35379534hg38UCSC Ensembl
Outerchr19:35358591..35383481hg38UCSC Ensembl
Innerchr19:35855353..35870436hg19UCSC Ensembl
Outerchr19:35849493..35874383hg19UCSC Ensembl
Innerchr19:40547193..40562276hg18UCSC Ensembl
Outerchr19:40541333..40566223hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3824891
hg1924891
hg1824891
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169895
Supporting Variants
SamplesNGO_47
Known GenesFFAR3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246845
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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