A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2978352



Internal ID15755498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:119754553..119756585hg38UCSC Ensembl
InnerchrX:118888516..118890548hg19UCSC Ensembl
InnerchrX:118772544..118774576hg18UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg382033
hg192033
hg182033
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515165
Supporting Variants
SamplesNA19185
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2978352
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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