A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513718



Internal ID15853139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:6216949..6220283hg38UCSC Ensembl
OuterchrX:6134990..6138324hg19UCSC Ensembl
OuterchrX:6144990..6148324hg18UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg383335
hg193335
hg183335
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626970
Samples1
Known GenesNLGN4X
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513718
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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