A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3673n100



Internal ID20155289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54786419..54837236hg38UCSC Ensembl
chr19:55297871..55348691hg19UCSC Ensembl
chr19:59989683..60040503hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3850818
hg1950821
hg1850821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066434, nsv1060742, nsv1056929, nsv1063966, nsv1059682
Samples
Known GenesKIR2DL4, KIR2DS4, KIR3DL1, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3673n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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