A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078701



Internal ID19322354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3708858..3726359hg38UCSC Ensembl
chrY:3576899..3594400hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3817502
hg1917502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766213
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078701
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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