A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9931



Internal ID15501157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:7264520..7270013hg38UCSC Ensembl
OuterchrX:7182561..7188054hg19UCSC Ensembl
OuterchrX:7192561..7198054hg18UCSC Ensembl
OuterchrX:7042297..7047790hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg385494
hg195494
hg185494
hg175494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26501
SamplesNA19173
Known GenesSTS
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)nsv9931
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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