A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969350



Internal ID18892356
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 StatusS
Merged Variantsnsv1133775
Supporting Variants
SamplesKWS2
Known GenesIRAK1, MIR718
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969350
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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