A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626861



Internal ID15850394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:66036580..66037936hg38UCSC Ensembl
OuterchrX:65256422..65257778hg19UCSC Ensembl
OuterchrX:65173147..65174503hg18UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38933
hg19933
hg18933
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513609
Supporting Variants
Samples1
Known GenesVSIG4
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626861
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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