A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1687n100



Internal ID22787774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63715171..63845046hg38UCSC Ensembl
chr13:64289304..64419179hg19UCSC Ensembl
chr13:63187305..63317180hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38129876
hg19129876
hg18129876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051772, nsv1047233
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)dgv1687n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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