A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5512n100



Internal ID22791599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15520..82468hg38UCSC Ensembl
chr5:15520..82583hg19UCSC Ensembl
chr5:68520..135583hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3866949
hg1967064
hg1867064
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029549, nsv1025253, nsv1029733
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5512n100
Frequency
Sample Size11257
Observed Gain14
Observed Loss3
Observed Complex0
Frequencyn/a


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