A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1686n100



Internal ID22787773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63673517..63807391hg38UCSC Ensembl
chr13:64247650..64381524hg19UCSC Ensembl
chr13:63145651..63279525hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38133875
hg19133875
hg18133875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036769, nsv1048543, nsv1039766, nsv1047128, nsv1042343, nsv1036826, nsv1047467, nsv1037077, nsv1040776, nsv1045902, nsv1041068, nsv1045624, nsv1037962, nsv1047712, nsv1042019, nsv1039682, nsv1046214
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1686n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss55
Observed Complex0
Frequencyn/a


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