A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893167



Internal ID18837301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14610447..14950404hg38UCSC Ensembl
Outerchr19:14610447..14950404hg38UCSC Ensembl
Innerchr19:14721259..15061216hg19UCSC Ensembl
Outerchr19:14721259..15061216hg19UCSC Ensembl
Innerchr19:14582259..14922216hg18UCSC Ensembl
Outerchr19:14582259..14922216hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38339958
hg19339958
hg18339958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790354
Samples
Known GenesCLEC17A, EMR2, EMR3, OR7A10, OR7A17, OR7A5, OR7C1, OR7C2, SLC1A6, ZNF333
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893167
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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