A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151837



Internal ID19197153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:151023726..151027728hg38UCSC Ensembl
OuterchrX:150192199..150196200hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg384003
hg194002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999021
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151837
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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