A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6426n54



Internal ID20139850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36353293..36356091hg38UCSC Ensembl
chr19:36844195..36846993hg19UCSC Ensembl
chr19:41536035..41538833hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382799
hg192799
hg182799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579438, nsv579435, nsv579434, nsv579439, nsv579433
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6426n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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