A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3667n100



Internal ID20155283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54725768..54862351hg38UCSC Ensembl
chr19:55237234..55373806hg19UCSC Ensembl
chr19:59929046..60065618hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38136584
hg19136573
hg18136573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057358, nsv1055990, nsv1061979, nsv1063393, nsv1058874, nsv1058654, nsv1064335, nsv1055639, nsv1061825, nsv1055826, nsv1057348, nsv1058380, nsv1062189
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, KIR3DL3, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3667n100
Frequency
Sample Size29084
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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