A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3679n100



Internal ID20155295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54944244..55017462hg38UCSC Ensembl
chr19:55455612..55528830hg19UCSC Ensembl
chr19:60147424..60220642hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3873219
hg1973219
hg1873219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057583, nsv1058841, nsv1066972
Samples
Known GenesGP6, NLRP2, NLRP7, RNU6-35P, RNU6-64P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3679n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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