A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1623n100



Internal ID22787710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26802474..26837226hg38UCSC Ensembl
chr13:27376611..27411363hg19UCSC Ensembl
chr13:26274611..26309363hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3834753
hg1934753
hg1834753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038055, nsv1041293, nsv1037959
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)dgv1623n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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