A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769784



Internal ID19310007
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 StatusS
Merged Variantsnsv1078158
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769784
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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