A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2891974



Internal ID15261769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151793730..151832482hg38UCSC Ensembl
Innerchr3:151511518..151550270hg19UCSC Ensembl
Innerchr3:152994208..153032960hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3838753
hg1938753
hg1838753
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514175
Supporting Variants
SamplesNA11829
Known GenesAADAC, MIR548H2
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2891974
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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