A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125445



Internal ID18935848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:72165142..72194553hg38UCSC Ensembl
OuterchrX:71384992..71414403hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3829412
hg1929412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983618
SamplesKWS2
Known GenesPIN4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125445
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