A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076657



Internal ID19319869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40284881..40339482hg38UCSC Ensembl
chr9:42429899..42484500hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3854602
hg1954602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769033
SamplesKWP1
Known GenesFAM95B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076657
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer