A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250103



Internal ID21304238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68628613..68648152hg38UCSC Ensembl
Outerchr17:68626761..68651699hg38UCSC Ensembl
Innerchr17:66624754..66644293hg19UCSC Ensembl
Outerchr17:66622902..66647840hg19UCSC Ensembl
Innerchr17:64136349..64155888hg18UCSC Ensembl
Outerchr17:64134497..64159435hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3824939
hg1924939
hg1824939
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170194
Supporting Variants
SamplesNGO_11
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250103
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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