A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075255



Internal ID18971164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95004717..95005018hg38UCSC Ensembl
chr9:97766999..97767300hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772588
SamplesKWP1
Known GenesC9orf3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075255
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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