A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125141



Internal ID19269537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:450065..516665hg38UCSC Ensembl
OuterchrY:360800..427400hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3866601
hg1966601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977947
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125141
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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