A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6302n54



Internal ID22774197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19727083..19728732hg38UCSC Ensembl
chr19:19837892..19839541hg19UCSC Ensembl
chr19:19698892..19700541hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381650
hg191650
hg181650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578797, nsv578795
Samples
Known GenesZNF14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6302n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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