A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6223n54



Internal ID22774118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2701559..2708339hg38UCSC Ensembl
chr19:2701557..2708337hg19UCSC Ensembl
chr19:2652557..2659337hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386781
hg196781
hg186781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578399, nsv578411
Samples
Known GenesGNG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6223n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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