A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2850064



Internal ID15315712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161443602..161481554hg38UCSC Ensembl
Innerchr1:161413392..161451344hg19UCSC Ensembl
Innerchr1:159680016..159717968hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3837953
hg1937953
hg1837953
Variant TypeCNV gain
Copy Number37
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514914
Supporting Variants
SamplesNA18487
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2850064
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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