A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076743



Internal ID19323475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10136890..10157591hg38UCSC Ensembl
chrY:9974499..9995200hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3820702
hg1920702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772851
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076743
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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