A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077115



Internal ID19316623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42644119..42661263hg38UCSC Ensembl
chr9:44309099..44327000hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3817145
hg1917902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771587
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077115
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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