A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150384



Internal ID19195741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:131679252..131840273hg38UCSC Ensembl
OuterchrX:130813266..130974301hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38161022
hg19161036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003684
SamplesKWB1
Known GenesLOC286467
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150384
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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