A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129110



Internal ID19258173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:245633..274833hg38UCSC Ensembl
OuterchrY:112300..141500hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3829201
hg1929201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961784
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129110
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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