A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078158



Internal ID19320426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:19936213..19945514hg38UCSC Ensembl
chrY:22098099..22107400hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg389302
hg199302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769784
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078158
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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