A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6198n54



Internal ID20139622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1249277..1250886hg38UCSC Ensembl
chr19:1249276..1250885hg19UCSC Ensembl
chr19:1200276..1201885hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381610
hg191610
hg181610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578277, nsv578275
Samples
Known GenesMIDN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6198n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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