A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26456



Internal ID15841523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:156021822..156028123hg38UCSC Ensembl
OuterchrX:156020254..156030895hg38UCSC Ensembl
InnerchrX:155251487..155257788hg19UCSC Ensembl
OuterchrX:155249919..155260560hg19UCSC Ensembl
InnerchrX:154904681..154910982hg18UCSC Ensembl
OuterchrX:154903113..154913754hg18UCSC Ensembl
InnerchrX:154815191..154821492hg17UCSC Ensembl
OuterchrX:154813623..154824264hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3810642
hg1910642
hg1810642
hg1710642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10003
Supporting Variants
SamplesNA19007
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)nssv26456
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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