A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512692



Internal ID15852117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:97601535..97657942hg38UCSC Ensembl
OuterchrX:96856534..96912941hg19UCSC Ensembl
OuterchrX:96743190..96799597hg18UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3856408
hg1956408
hg1856408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv64n50
Supporting Variantsnssv625314
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512692
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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