A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075673



Internal ID19323852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126860620..126860921hg38UCSC Ensembl
chr9:129622899..129623200hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767479
SamplesKWP1
Known GenesZBTB34
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075673
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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