A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077545



Internal ID19320661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63303527..63356528hg38UCSC Ensembl
chr9:67258499..67311500hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3853002
hg1953002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763688
SamplesKWP1
Known GenesAQP7P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077545
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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