A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135388



Internal ID19253064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:95795801..95796501hg38UCSC Ensembl
OuterchrX:95050800..95051500hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4269n106
Supporting Variantsnssv3962949, nssv3966181
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135388
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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