A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1609n100



Internal ID20153225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19822918..19936310hg38UCSC Ensembl
chr13:20397058..20510450hg19UCSC Ensembl
chr13:19295058..19408450hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38113393
hg19113393
hg18113393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049946, nsv1051774
Samples
Known GenesZMYM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1609n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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