A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076744



Internal ID19322364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10176890..10184991hg38UCSC Ensembl
chrY:10014499..10022600hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg388102
hg198102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765018
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076744
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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