A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3604n100



Internal ID22789691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43414688..43453235hg38UCSC Ensembl
chr19:43918840..43957387hg19UCSC Ensembl
chr19:48610680..48649227hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3838548
hg1938548
hg1838548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066231, nsv1061862, nsv1058848
Samples
Known GenesTEX101
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3604n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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