A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078161



Internal ID18976249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21493813..21551514hg38UCSC Ensembl
chrY:23655699..23713400hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3857702
hg1957702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762615
SamplesKWP1
Known GenesRBMY1A1, RBMY1B, RBMY1D, RBMY1E
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078161
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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