A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077170



Internal ID18971185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109166719..109167420hg38UCSC Ensembl
chr9:111928999..111929700hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768561
SamplesKWP1
Known GenesFRRS1L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077170
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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