A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112213



Internal ID19254689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11310406..11329841hg38UCSC Ensembl
OuterchrY:13466082..13485517hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3819436
hg1919436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4347n106
Supporting Variantsnssv3965911
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112213
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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