A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252503



Internal ID21307194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104427454..104497800hg38UCSC Ensembl
Outerchr13:104422616..104500724hg38UCSC Ensembl
Innerchr13:105079804..105150150hg19UCSC Ensembl
Outerchr13:105074966..105153074hg19UCSC Ensembl
Innerchr13:103877805..103948151hg18UCSC Ensembl
Outerchr13:103872967..103951075hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3878109
hg1978109
hg1878109
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169428
Supporting Variants
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252503
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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