A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511652



Internal ID15504391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155551990..155566796hg38UCSC Ensembl
OuterchrX:155551462..155586778hg38UCSC Ensembl
InnerchrX:154781651..154796457hg19UCSC Ensembl
OuterchrX:154781123..154816439hg19UCSC Ensembl
InnerchrX:154434845..154449651hg18UCSC Ensembl
OuterchrX:154434317..154469633hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3835317
hg1935317
hg1835317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626287
Samples1
Known GenesTMLHE
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511652
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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