A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3676n100



Internal ID20155292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54786419..54868189hg38UCSC Ensembl
chr19:55297871..55379644hg19UCSC Ensembl
chr19:59989683..60071456hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3881771
hg1981774
hg1881774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067347, nsv1055552, nsv1056214, nsv1057709, nsv1057812, nsv1059664, nsv1064480, nsv1060713, nsv1056921, nsv1058728, nsv1064786, nsv1056495, nsv1063667, nsv1056092, nsv1067502, nsv1061865
Samples
Known GenesKIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3676n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss52
Observed Complex0
Frequencyn/a


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