A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125152



Internal ID19262496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10218691..10233691hg38UCSC Ensembl
OuterchrY:10056300..10071300hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3815001
hg1915001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977958
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125152
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