A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1604n100



Internal ID22787691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18600494..18737640hg38UCSC Ensembl
chr13:19174634..19311780hg19UCSC Ensembl
chr13:18072634..18209780hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38137147
hg19137147
hg18137147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042239, nsv1042350, nsv1037534
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)dgv1604n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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