A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078720



Internal ID19319324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56821552..56886953hg38UCSC Ensembl
chrY:58967699..59033100hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3865402
hg1965402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770166
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078720
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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