A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141721



Internal ID19266824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:340465..377065hg38UCSC Ensembl
OuterchrY:251200..287800hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3836601
hg1936601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993227
SamplesKWS2
Known GenesPPP2R3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141721
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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