A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151231



Internal ID19202039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11272123..11285424hg38UCSC Ensembl
OuterchrY:13427799..13441100hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3813302
hg1913302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003796
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151231
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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