A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075283



Internal ID19316634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136033353..136055154hg38UCSC Ensembl
chr9:138925199..138947000hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3821802
hg1921802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769014
SamplesKWP1
Known GenesNACC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075283
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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