A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2984494



Internal ID15676921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:37825899..37850187hg38UCSC Ensembl
InnerchrX:37685152..37709440hg19UCSC Ensembl
InnerchrX:37570096..37594384hg18UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3824289
hg1924289
hg1824289
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515194
Supporting Variants
SamplesNA18558
Known GenesDYNLT3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2984494
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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