A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626881



Internal ID15503728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:152182709..152182807hg38UCSC Ensembl
OuterchrX:151351181..151351279hg19UCSC Ensembl
OuterchrX:151101837..151101935hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38931
hg19931
hg18931
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513629
Supporting Variants
Samples1
Known GenesGABRA3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626881
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer