A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9956



Internal ID15847868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:82127265..82163413hg38UCSC Ensembl
OuterchrX:81382714..81418862hg19UCSC Ensembl
OuterchrX:81269370..81305518hg18UCSC Ensembl
OuterchrX:81188859..81225007hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3836149
hg1936149
hg1836149
hg1736149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27573
SamplesNA18504
Known Genes
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)nsv9956
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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