A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115314



Internal ID19254388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11379976..11380051hg38UCSC Ensembl
OuterchrY:13535652..13535727hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4349n106
Supporting Variantsnssv3976364
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115314
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