A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512566



Internal ID15851991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19722377..19729378hg38UCSC Ensembl
Outerchr19:19833186..19840187hg19UCSC Ensembl
Outerchr19:19694186..19701187hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg387002
hg197002
hg187002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625174
Samples1
Known GenesZNF14
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512566
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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