A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6304n54



Internal ID20139728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20379052..20638696hg38UCSC Ensembl
chr19:20489861..20821502hg19UCSC Ensembl
chr19:20350861..20613342hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38259645
hg19331642
hg18262482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578816, nsv578818, nsv578831, nsv578817, nsv578819, nsv578811, nsv578832
SamplesHGDP01237, HGDP00205
Known GenesMIR1270-1, MIR1270-2, ZNF626, ZNF737, ZNF826P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6304n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer