A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133775



Internal ID18916052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154019649..154020049hg38UCSC Ensembl
OuterchrX:153285100..153285500hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969350
SamplesKWS2
Known GenesIRAK1, MIR718
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133775
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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