A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978663



Internal ID19227248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:131679249..131840269hg38UCSC Ensembl
OuterchrX:130813263..130974297hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38161021
hg19161035
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116482
Supporting Variants
SamplesKWS2
Known GenesLOC286467
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978663
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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