A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1624n100



Internal ID22787711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30831285..30864668hg38UCSC Ensembl
chr13:31405422..31438805hg19UCSC Ensembl
chr13:30303422..30336805hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3833384
hg1933384
hg1833384
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044885, nsv1049279, nsv1043834, nsv1035645, nsv1048702
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)dgv1624n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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