A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137704



Internal ID19274271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:280133..281433hg38UCSC Ensembl
OuterchrY:146800..148100hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990204
SamplesKWS2
Known GenesPLCXD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137704
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