A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077550



Internal ID18970842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63767865..63844166hg38UCSC Ensembl
chr9:68363599..68439900hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3876302
hg1976302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767505
SamplesKWP1
Known GenesLOC642236
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077550
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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