A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962902



Internal ID19211665
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 StatusS
Merged Variantsnsv1129450
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962902
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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