A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075207



Internal ID18972598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41817867..41900729hg38UCSC Ensembl
chr9:40330699..40416800hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3882863
hg1986102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768946
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075207
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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