A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9958



Internal ID15501184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:84065589..84070603hg38UCSC Ensembl
OuterchrX:83320597..83325611hg19UCSC Ensembl
OuterchrX:83207253..83212267hg18UCSC Ensembl
OuterchrX:83126742..83131756hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg385015
hg195015
hg185015
hg175015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23525
SamplesNA18572
Known GenesRPS6KA6
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv9958
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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