A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2842946



Internal ID15424662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36350230..36355994hg38UCSC Ensembl
Innerchr19:36841132..36846896hg19UCSC Ensembl
Innerchr19:41532972..41538736hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385765
hg195765
hg185765
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514898
Supporting Variants
SamplesNA19248
Known GenesZFP14
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2842946
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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