A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140092



Internal ID18916323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:6240259..6261759hg38UCSC Ensembl
OuterchrY:6108300..6129800hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3821501
hg1921501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4339n106
Supporting Variantsnssv3978803
SamplesKWS2
Known GenesTSPY2, TTTY23, TTTY23B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140092
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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