A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151900



Internal ID19200492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10197190..10203491hg38UCSC Ensembl
OuterchrY:10034799..10041100hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg386302
hg196302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999084
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151900
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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