A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115321



Internal ID19263460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56829352..56829432hg38UCSC Ensembl
OuterchrY:58975499..58975579hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4368n106
Supporting Variantsnssv3976373
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115321
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