A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150780



Internal ID19195755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56838214..56851297hg38UCSC Ensembl
OuterchrY:58984361..58997444hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3813084
hg1913084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996254
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150780
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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