A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512683



Internal ID15852108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:81840846..81847671hg38UCSC Ensembl
OuterchrX:81096345..81103170hg19UCSC Ensembl
OuterchrX:80983001..80989826hg18UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg386826
hg196826
hg186826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625304
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)nsv512683
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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