A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076654



Internal ID19319853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39753581..39839882hg38UCSC Ensembl
chr9:41898599..41984900hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3886302
hg1986302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771970
SamplesKWP1
Known GenesKGFLP2, MGC21881
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076654
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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