A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145902



Internal ID19202856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:42888550..42894151hg38UCSC Ensembl
OuterchrX:42747799..42753400hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg385602
hg195602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997265
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1145902
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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