A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2902801



Internal ID15409134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150960694..150962630hg38UCSC Ensembl
Innerchr4:151881846..151883782hg19UCSC Ensembl
Innerchr4:152101296..152103232hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg381937
hg191937
hg181937
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514258
Supporting Variants
SamplesNA19186
Known GenesLRBA
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2902801
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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