A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2982172



Internal ID15688843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:150062391..150081511hg38UCSC Ensembl
InnerchrX:149230622..149249742hg19UCSC Ensembl
InnerchrX:148981280..149000400hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3819121
hg1919121
hg1819121
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515183
Supporting Variants
SamplesNA18632
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2982172
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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