A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3423n100



Internal ID22789510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7156726..7275281hg38UCSC Ensembl
chr19:7156737..7275292hg19UCSC Ensembl
chr19:7107737..7226292hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38118556
hg19118556
hg18118556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065352, nsv1058527, nsv1067058
Samples
Known GenesINSR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3423n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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