A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075213



Internal ID19318114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66204221..66207722hg38UCSC Ensembl
chr9:43184799..43188300hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg383502
hg193502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772648
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075213
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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