A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2855037



Internal ID15651942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:209904688..209912848hg38UCSC Ensembl
Innerchr1:210078033..210086193hg19UCSC Ensembl
Innerchr1:208144656..208152816hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg388161
hg198161
hg188161
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514039
Supporting Variants
SamplesNA12818
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2855037
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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