A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110872



Internal ID19277978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:131678467..131841236hg38UCSC Ensembl
OuterchrX:130812480..130975264hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38162770
hg19162785
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4293n106
Supporting Variantsnssv3961283
SamplesKWS1
Known GenesLOC286467
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110872
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer