A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3529n100



Internal ID20155145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39633228..39820356hg38UCSC Ensembl
chr19:40123868..40310996hg19UCSC Ensembl
chr19:44815708..45002836hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38187129
hg19187129
hg18187129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061361, nsv1057361
Samples
Known GenesCLC, LEUTX, LGALS14, LGALS16, LGALS17A, LOC100129935
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3529n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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