A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511663



Internal ID15504402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155688696..155691896hg38UCSC Ensembl
OuterchrX:155687184..155709357hg38UCSC Ensembl
InnerchrX:154918357..154921557hg19UCSC Ensembl
OuterchrX:154916845..154939018hg19UCSC Ensembl
InnerchrX:154571551..154574751hg18UCSC Ensembl
OuterchrX:154570039..154592212hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3822174
hg1922174
hg1822174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626300
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511663
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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