A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076689



Internal ID18979737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135835953..135839154hg38UCSC Ensembl
chr9:138727799..138731000hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383202
hg193202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772589
SamplesKWP1
Known GenesCAMSAP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076689
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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