A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2839174



Internal ID15600931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19727215..19728871hg38UCSC Ensembl
Innerchr19:19838024..19839680hg19UCSC Ensembl
Innerchr19:19699024..19700680hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381657
hg191657
hg181657
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514892
Supporting Variants
SamplesNA10839
Known GenesZNF14
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2839174
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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