A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245590



Internal ID21310163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89487306..89497867hg38UCSC Ensembl
Outerchr3:89475943..89503594hg38UCSC Ensembl
Innerchr3:89536456..89547017hg19UCSC Ensembl
Outerchr3:89525093..89552744hg19UCSC Ensembl
Innerchr3:89619146..89629707hg18UCSC Ensembl
Outerchr3:89607783..89635434hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3827652
hg1927652
hg1827652
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169818
Supporting Variants
SamplesNGO_55
Known GenesEPHA3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245590
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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