A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170307



Internal ID21314368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36202820..36205283hg38UCSC Ensembl
Outerchr14:36200198..36210414hg38UCSC Ensembl
Innerchr14:36672026..36674489hg19UCSC Ensembl
Outerchr14:36669404..36679620hg19UCSC Ensembl
Innerchr14:35741777..35744240hg18UCSC Ensembl
Outerchr14:35739155..35749371hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3810217
hg1910217
hg1810217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245470
SamplesNGO_51
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170307
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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