A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078693



Internal ID18970871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155516238..155519139hg38UCSC Ensembl
chrX:154745899..154748800hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg382902
hg192902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764371
SamplesKWP1
Known GenesTMLHE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078693
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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