A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2983840



Internal ID15321323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155563801..155567513hg38UCSC Ensembl
InnerchrX:154793462..154797174hg19UCSC Ensembl
InnerchrX:154446656..154450368hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg383713
hg193713
hg183713
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515187
Supporting Variants
SamplesNA18508
Known GenesTMLHE
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2983840
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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