A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625314



Internal ID15848850
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 StatusS
Merged Variantsnsv512692
Supporting Variants
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)nssv625314
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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