A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1601n100



Internal ID22787688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18471488..18824655hg38UCSC Ensembl
chr13:19045628..19398795hg19UCSC Ensembl
chr13:17943628..18296795hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38353168
hg19353168
hg18353168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044149, nsv1054926
Samples
Known GenesLINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1601n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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