A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1117920



Internal ID19262478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11295515..11296578hg38UCSC Ensembl
OuterchrY:13451191..13452254hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg381064
hg191064
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980122, nssv3988462
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1117920
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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