A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149110



Internal ID19198579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:57206748..57209749hg38UCSC Ensembl
OuterchrY:59352899..59355900hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002620
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149110
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer