A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132810



Internal ID19250388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11179524..11349624hg38UCSC Ensembl
OuterchrY:13335200..13505300hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg38170101
hg19170101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987602
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132810
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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