A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762825



Internal ID18962199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:43670851..43675252hg38UCSC Ensembl
chrX:43530099..43534500hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg384402
hg194402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078108
Supporting Variants
SamplesKWP1
Known GenesMAOA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762825
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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