A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077533



Internal ID19316356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64461211..64505575hg38UCSC Ensembl
chr9:42991399..43035700hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3844365
hg1944302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765159
SamplesKWP1
Known GenesFAM95B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077533
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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