A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2987725



Internal ID15624954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24181996..24182710hg38UCSC Ensembl
InnerchrX:24200113..24200827hg19UCSC Ensembl
InnerchrX:24110034..24110748hg18UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38715
hg19715
hg18715
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515191
Supporting Variants
SamplesNA12239
Known GenesZFX
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2987725
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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