A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5513n100



Internal ID22791600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15520..106980hg38UCSC Ensembl
chr5:15520..107095hg19UCSC Ensembl
chr5:68520..160095hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3891461
hg1991576
hg1891576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029868, nsv1016202, nsv1030666, nsv1022531
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)dgv5513n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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