A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765170



Internal ID18964802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103014735..103014836hg38UCSC Ensembl
chr9:105777017..105777118hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075668
Supporting Variants
SamplesKWP1
Known GenesCYLC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765170
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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