A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2843645



Internal ID15737611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9752742..9760415hg38UCSC Ensembl
Innerchr19:9863418..9871091hg19UCSC Ensembl
Innerchr19:9724418..9732091hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387674
hg197674
hg187674
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514908
Supporting Variants
SamplesNA19127
Known GenesZNF846
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2843645
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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