A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3671n100



Internal ID20155287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54736428..54837236hg38UCSC Ensembl
chr19:55247895..55348691hg19UCSC Ensembl
chr19:59939707..60040503hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38100809
hg19100797
hg18100797
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066237, nsv1066264, nsv1066413, nsv1066866, nsv1067104, nsv1055184
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR2DS4, KIR3DL1, 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)dgv3671n100
Frequency
Sample Size29084
Observed Gain26
Observed Loss41
Observed Complex0
Frequencyn/a


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