A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1777n106



Internal ID20161134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36349798..36356198hg38UCSC Ensembl
chr19:36840700..36847100hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386401
hg196401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110403, nsv1130800, nsv1144845
SamplesKWS1
Known GenesZFP14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1777n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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