A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3512n100



Internal ID19013880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29974636..30013166hg38UCSC Ensembl
chr19:30465543..30504073hg19UCSC Ensembl
chr19:35157383..35195913hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3838531
hg1938531
hg1838531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064709, nsv1061780
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3512n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer