A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3678n100



Internal ID20155294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54828266..54867232hg38UCSC Ensembl
chr19:55339721..55378687hg19UCSC Ensembl
chr19:60031533..60070499hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3838967
hg1938967
hg1838967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058239, nsv1055627
Samples
Known GenesKIR2DS4, KIR3DL1, KIR3DL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3678n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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