A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511664



Internal ID15851089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:127465389..127468239hg38UCSC Ensembl
OuterchrX:127459928..127470702hg38UCSC Ensembl
InnerchrX:126599370..126602220hg19UCSC Ensembl
OuterchrX:126593909..126604683hg19UCSC Ensembl
InnerchrX:126427051..126429901hg18UCSC Ensembl
OuterchrX:126421590..126432364hg18UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3810775
hg1910775
hg1810775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626301
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)nsv511664
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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