A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243618



Internal ID21304107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358591..35370946hg38UCSC Ensembl
Outerchr19:35358420..35375842hg38UCSC Ensembl
Innerchr19:35849493..35861848hg19UCSC Ensembl
Outerchr19:35849322..35866744hg19UCSC Ensembl
Innerchr19:40541333..40553688hg18UCSC Ensembl
Outerchr19:40541162..40558584hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3817423
hg1917423
hg1817423
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169895
Supporting Variants
SamplesNGO_10
Known GenesFFAR3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243618
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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