A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129450



Internal ID19284286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:84807866..84818854hg38UCSC Ensembl
OuterchrX:84062873..84073861hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3810989
hg1910989
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962902
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129450
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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