A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6268n54



Internal ID18998444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11930017..11934386hg38UCSC Ensembl
chr19:12040832..12045201hg19UCSC Ensembl
chr19:11901832..11906201hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384370
hg194370
hg184370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578620, nsv578621, nsv578622
Samples
Known GenesZNF700
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6268n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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